510(k) · Cleared

Cleared

Anybattery C2 Rechargeable Battery

K160667510(k) TraditionalCleared May 11, 2017428-day reviewClass II21 CFR 870.2340

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Anybattery, Inc. · DPS Electrocardiograph

Cleared on May 11, 2017 as substantially equivalent to K913484 (Zmi Corp., 1991) and 26 other predicates after a 428-day review. Its family tree reaches back 7 generations to 1997. 1 of the 78 devices in its family, counting itself, has a Class I recall.

Decided: May 11, 2017
Review: 428 days
Class: Class II
Product code: DPS
Recalls: None
Predicates: 27

Its longest line of descent runs back 7 generations to K962603 (1997). 77 ancestors in all, the oldest K760160 (1976). No later device cites it as a predicate yet. 1 of the 78 devices in this family, counting this one, has a Class I recall.

By dateBy generation

Root · 7 generations backK962603 Masimo Set MS-1 Pulse Oximeter & the Lnop Series of Sensors & CablesMasimo Corp. · 1997
6 generations backK973887 Masimo Set MS-1P Pulse Oximeter and the Lnop Series of Sensors and…Masimo Corp. · 1998
5 generations backK982255 Model 2000 Pulse OximeterIvy Biomedical Systems, Inc. · 1998
4 generations backK991823 N-395 Pulse Oximeter, Model N-395Nellcor Puritan Bennett, Inc. · 1999
3 generations backK012891 Oximax Pulse Oximetry System with N-595 Pulse Oximeter and Oximax…Nellcor Puritan Bennett, Inc. · 2002 · Recalled
2 generations backK021090 Oximax N-550 Pulse Oximeter,Model N-550 Pulse OximeterNellcor Puritan Bennett, Inc. · 2002
1 generation backK033048 Cas 740 Series Monitor, Models 740-1, 740M-1, 740-2MS, 740M-2MS…Cas Medical Systems, Inc. · 2004 · Recalled
This deviceK160667 Anybattery C2 Rechargeable BatteryAnybattery, Inc. · 2017

Class I recalls in this family

K970209 Capnocheck Plus2 generations back · 1997

View FIG. 1 as a table

Line of descent and top descendants

Generation	Number	Device	Applicant	Decided	Recalls
−7	K962603	Masimo Set MS-1 Pulse Oximeter & the Lnop Series of Sensors & Cables	Masimo Corp.	1997	—
−6	K973887	Masimo Set MS-1P Pulse Oximeter and the Lnop Series of Sensors and Cables	Masimo Corp.	1998	—
−5	K982255	Model 2000 Pulse Oximeter	Ivy Biomedical Systems, Inc.	1998	—
−4	K991823	N-395 Pulse Oximeter, Model N-395	Nellcor Puritan Bennett, Inc.	1999	—
−3	K012891	Oximax Pulse Oximetry System with N-595 Pulse Oximeter and Oximax Sensors and…	Nellcor Puritan Bennett, Inc.	2002	1
−2	K021090	Oximax N-550 Pulse Oximeter,Model N-550 Pulse Oximeter	Nellcor Puritan Bennett, Inc.	2002	—
−1	K033048	Cas 740 Series Monitor, Models 740-1, 740M-1, 740-2MS, 740M-2MS, 740-2NL…	Cas Medical Systems, Inc.	2004	1
0 (this device)	K160667	Anybattery C2 Rechargeable Battery	Anybattery, Inc.	2017	—

Other ancestors by year cleared

Year cleared	Devices	With a Class I recall
1976	1	0
1982	1	0
1984	1	0
1986	1	0
1987	2	0
1988	1	0
1989	1	0
1990	3	0
1991	6	0
1992	3	0
1993	5	0
1994	3	0
1995	6	0
1996	4	0
1997	6	1
1998	6	0
1999	7	0
2000	2	0
2001	2	0
2002	2	0
2003	1	0
2005	1	0
2006	2	0
2007	1	0
2010	1	0
2014	1	0

FIG. 1 — Lineage of K160667, 1997–2017Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

1 device in this family has a Class I recall. A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new DPS device

#1 K212112 Cardiologs Holter Platformscore 18.6 · 5 generations · no Class I recall
#2 Held for the reportin the report
#3 Held for the reportin the report

Get a 510(k) Report

What was it cleared against? (27)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

Type	Number	Device	Applicant	Decided	Recalls
*	K913484	Zoll D-900 Defibrillator Summary page 3 …Rechargeable Batteries in the VRLA Product Family. 1. Anybattery 3394 is substantial equivalent to that manufactured by: • Zoll D-900 defibrillator cleared K913484. 2. Anybattery 4028 is substantial equivalent to that manufactured by: • Hewlett-Packard Pagewriter XLI M1700A & Page…	Zmi Corp.	1991	—
*	K895520	Pagewriter Xli M1700A & Pagewriter XL M1701A Summary page 3 …4. 2. Anybattery 4028 is substantial equivalent to that manufactured by: • Hewlett-Packard Pagewriter XLI M1700A & Pagewriter XL M1701A cleared K895520. 3. Anybattery 4040 is substantial equivalent to that manufactured by: • HP 43100 series defibrillator monitors clear…	Hewlett-Packard Co.	1990	—
*	K910754	Model 43100A Series Defibrillator, Modification Summary page 3 …M1701A cleared K895520. 3. Anybattery 4040 is substantial equivalent to that manufactured by: • HP 43100 series defibrillator monitors cleared K910754. 4. Anybattery 4043 is substantial equivalent to that manufactured by: • Hewlett-Packard Monitor, Patient Model 78333…	Hewlett-Packard Co.	1991	—
*	K760160	Monitor, Patient (Model 78333A) Summary page 3 …lator monitors cleared K910754. 4. Anybattery 4043 is substantial equivalent to that manufactured by: • Hewlett-Packard Monitor, Patient Model 78333A cleared K760160. 5. Anybattery 4494 is substantial equivalent to that manufactured by: x Physio-Control LifePak 9 Defibrillator & Ca…	Hewlett-Packard Co.	1976	—
*	K881153	Lifepak 9 Defibrillator and Cardiac Monitor Summary page 3 …3A cleared K760160. 5. Anybattery 4494 is substantial equivalent to that manufactured by: x Physio-Control LifePak 9 Defibrillator & Cardiac Monitor cleared K881153. 6. Anybattery 4494-2 is substantial equivalent to that manufactured by: x Physio-Control LifePak 9 series defibrill…	Physio-Control Corp.	1988	1
*	K902288	Modified Lifepak 9 Monitor/Defibrillator Summary page 3 …or cleared K881153. 6. Anybattery 4494-2 is substantial equivalent to that manufactured by: x Physio-Control LifePak 9 series defibrillator monitors cleared K902288. 7. Anybattery 4510 is substantial substantially equivalent to that manufactured by: • Welch Allyn Protocol Propaq c…	Physio-Control Corp.	1991	2
*	K012451	Propaq Encore Models 202, 204, 206; Propaq CS Models 242, 244, 246 Summary page 3 …rillator monitors cleared K902288. 7. Anybattery 4510 is substantial substantially equivalent to that manufactured by: • Welch Allyn Protocol Propaq cleared K012451. 8. Anybattery 4713-2 is substantial equivalent to that manufactured by: x Physio-Control Lifepak 10 defibrillator c…	Welch Allyn Protocol, Inc.	2001	—
*	K931053	Lifepak 10 Defibrillator/Monitor W/Opt Pacemaker Summary page 3 …n Protocol Propaq cleared K012451. 8. Anybattery 4713-2 is substantial equivalent to that manufactured by: x Physio-Control Lifepak 10 defibrillator cleared K931053. 9. Anybattery 5349-4 is substantial equivalent to that manufactured by: • Nihon-Kohden TEC-7511A/TEC-7521A CardioLi…	Physio-Control Corp.	1993	—
*	K971436	Nihon Kohden Tec-7511A/Tec-7521A Cardiolife Portable Defibrillator and Accessories Summary page 3 …y 5349-4 is substantial equivalent to that manufactured by: • Nihon-Kohden TEC-7511A/TEC-7521A CardioLife Portable Defibrillator & Accessories cleared K971436. 10. Anybattery 6558 is e substantial equivalent to that manufactured by: • Spacelabs Healthcare Telemetry Receiver…	Nihon Kohden America, Inc.	1997	—
*	K141156	Spacelabs Healthcare Telemetry Receiver Summary page 3 …Accessories cleared K971436. 10. Anybattery 6558 is e substantial equivalent to that manufactured by: • Spacelabs Healthcare Telemetry Receiver cleared K141156 & K925510. 11. Anybattery 7714-1 and 7714-2 are substantial equivalent to that manufactured by: • Colin Pressmate PM2…	Spacelabs Healthcare	2014	6
*	K925510	Model 90478 & 90479 Telemetry Rec. Module&Housing Summary page 3 …sories cleared K971436. 10. Anybattery 6558 is e substantial equivalent to that manufactured by: • Spacelabs Healthcare Telemetry Receiver cleared K141156 & K925510. 11. Anybattery 7714-1 and 7714-2 are substantial equivalent to that manufactured by: • Colin Pressmate PM2100 VSM cl…	Spacelabs Medical, Inc.	1994	2
*	K022537	Press-Mate PM-2100 Vital Sign Monitor Summary page 3 …Receiver cleared K141156 & K925510. 11. Anybattery 7714-1 and 7714-2 are substantial equivalent to that manufactured by: • Colin Pressmate PM2100 VSM cleared K022537. 12. Anybattery 8601 is substantial equivalent to that manufactured by: • Welch Allyn Atlus Monitor cleared K984033.…	Colin Medical Instruments Corp.	2002	—
*	K984033	Atlas Monitor Summary page 3 …• Colin Pressmate PM2100 VSM cleared K022537. 12. Anybattery 8601 is substantial equivalent to that manufactured by: • Welch Allyn Atlus Monitor cleared K984033. Page 4 – Claude Berthoin Anybattery C2 Rechargeable Batteries in the Nickel-Based Rechargeable Battery…	Welch Allyn, Inc.	1999	—
*	K870880	EK10 Electrocardiograph Summary page 4 …Nickel-Based Rechargeable Battery Product Family 1. Anybattery 3777 is substantial equivalent to that manufactured by: • Burdick EK10 Series ECG cleared K870880. 2. Anybattery 4218 is substantial equivalent to that manufactured by • General Electric MAC Series Electrocardiogra…	Burdick Corp.	1987	—
*	K991735	Mac Series Electrocardiographs Including Mac 5000, Mac PC, Mac 6, Mac VU, Mac 8… Summary page 4 …0 Series ECG cleared K870880. 2. Anybattery 4218 is substantial equivalent to that manufactured by • General Electric MAC Series Electrocardiographs cleared K991735. 3. Anybattery 4227 is substantial equivalent to that manufactured by: • Marquette Eagle 4000 Patient Monitor clea…	General Electric Medical Systems Information Techn	1999	—
*	K964750	Eagle 4000 Patient Monitor Summary page 4 …Electrocardiographs cleared K991735. 3. Anybattery 4227 is substantial equivalent to that manufactured by: • Marquette Eagle 4000 Patient Monitor cleared K964750. 4. Anybattery 5960 is substantial equivalent to that manufactured by: • Schiller AT-5 cleared K941462. 5. Anyb…	Marquette Electronics, Inc.	1997	—
*	K941462	Cardiovit at-5C Summary page 4 …• Marquette Eagle 4000 Patient Monitor cleared K964750. 4. Anybattery 5960 is substantial equivalent to that manufactured by: • Schiller AT-5 cleared K941462. 5. Anybattery 6459, 7062-1 and 7062-2 are substantial equivalent to that manufactured by: • Burdick Eclipse Series…	Schiller America, Inc.	1995	—
*	K943959	Eclipse 4 Electrocardiograph Summary page 4 …chiller AT-5 cleared K941462. 5. Anybattery 6459, 7062-1 and 7062-2 are substantial equivalent to that manufactured by: • Burdick Eclipse Series ECG cleared K943959 & K946281. 6. Anybattery 7023 is substantial equivalent to that manufactured by: • General Electric MAC Series Elec…	Burdick, Inc.	1995	—
*	K946281	Eclipse 4 Electrocardiograph Summary page 4 …-5 cleared K941462. 5. Anybattery 6459, 7062-1 and 7062-2 are substantial equivalent to that manufactured by: • Burdick Eclipse Series ECG cleared K943959 & K946281. 6. Anybattery 7023 is substantial equivalent to that manufactured by: • General Electric MAC Series Electrocardiog…	Burdick, Inc.	1996	—
*	K102422	Spacelabs Medical Patient Monitors Summary page 4 …ies Electrocardiographs cleared K991735. 7. Anybattery 7038 is substantial equivalent to that manufactured by: • Spacelabs Medical Patient Monitors cleared K102422. 8. Anybattery 7050 is substantial equivalent to that manufactured by: • Critikon Dinamap Pro 1000 Monitor cleared…	Spacelabs Medical, Inc.	2010	3
*	K002248	Dinamap Pro 1000 Monitor, Model 1000 Summary page 4 …Medical Patient Monitors cleared K102422. 8. Anybattery 7050 is substantial equivalent to that manufactured by: • Critikon Dinamap Pro 1000 Monitor cleared K002248. 9. Anybattery 7059 is substantial equivalent to that manufactured by: • BCI Intl., Inc. 6004 NIBP Monitor cleared…	Critikon Company, LLC	2000	—
*	K983796	6004 Nibp Monitor with Temperature Summary page 4 …Dinamap Pro 1000 Monitor cleared K002248. 9. Anybattery 7059 is substantial equivalent to that manufactured by: • BCI Intl., Inc. 6004 NIBP Monitor cleared K983796 & K984618. 10. Anybattery 7171 is substantial equivalent to that manufactured by: • Nihon Kohden ECG-1250A Series…	Bci Intl., Inc.	1999	1
*	K984618	Bci Mini-Torr Plus, Model 6004 Summary page 4 …o 1000 Monitor cleared K002248. 9. Anybattery 7059 is substantial equivalent to that manufactured by: • BCI Intl., Inc. 6004 NIBP Monitor cleared K983796 & K984618. 10. Anybattery 7171 is substantial equivalent to that manufactured by: • Nihon Kohden ECG-1250A Series and ECG-13…	Bci Intl., Inc.	1999	1
*	K072217	Ecg-1250A Series Cardiofax S and Ecg-1350A Series Cardiofax M Summary page 4 …84618. 10. Anybattery 7171 is substantial equivalent to that manufactured by: • Nihon Kohden ECG-1250A Series and ECG-1350A Series ECGs cleared K072217. 11. Anybattery 7711 is substantial equivalent to that manufactured by: • Nihon Kohden BSM-2300A Series Bedside Mo…	Nihon Kohden America, Inc.	2007	—
*	K011918	Nihon Kohden BSM-2300A Series Bedside Monitor and Accessories, Model BSM-2300A Series Summary page 4 …cleared K072217. 11. Anybattery 7711 is substantial equivalent to that manufactured by: • Nihon Kohden BSM-2300A Series Bedside Monitor cleared K011918. 12. Anybattery 7726 is substantial equivalent to that manufactured by • CAS Medical 740 Series Monitor cleared K033…	Nihon Kohden America, Inc.	2001	—
*	K033048	Cas 740 Series Monitor, Models 740-1, 740M-1, 740-2MS, 740M-2MS, 740-2NL, 740M-2NL… Summary page 4 …2300A Series Bedside Monitor cleared K011918. 12. Anybattery 7726 is substantial equivalent to that manufactured by • CAS Medical 740 Series Monitor cleared K033048. 13. Anybattery 7732 is substantial equivalent to that manufactured by: • Cardiac Science Atria 3100, 6100 cleared K…	Cas Medical Systems, Inc.	2004	1
*	K060167	Atria 3100, Atria 6100 Summary page 4 …edical 740 Series Monitor cleared K033048. 13. Anybattery 7732 is substantial equivalent to that manufactured by: • Cardiac Science Atria 3100, 6100 cleared K060167. DEPARTMENT OF HEALTH AND HUMAN SERVICES Form Approved: OMB N…	Cardiac Science Corporation	2006	—

What descends from it?

No later submission names this one as a predicate yet.

Has anything in its family been recalled? (1 Class I)

No FDA recall names this device.

Relatives with a Class I recall

Class I is FDA’s most serious recall class. A recall in the family tree is context for this device, not evidence about it.

K970209Capnocheck PlusBci Intl., Inc. · 1997 · 2 generations back · ◆ in the 1997 ancestors bar of FIG. 11 Class I recall

What does this lineage say?

The line of descent spans 20 years and passes through 5 companies; a new generation was cleared every 11 months on median.
17 of the 77 ancestors have a recall of any class; 1 has a Class I recall.

How does its category compare?

All DPS devices

DPS Electrocardiograph: FDA decisions, review times, recalls and adverse event reports over 20 years. 2017, this device’s year, is highlighted.

FDA decisions per year · DPS

6in 2025

2007high 22 (2011) · low 3 (2019)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · DPS

163in 2025

2007high 260 (2024) · low 31 (2008)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · DPS

3in 2025

2007high 9 (2019) · low 0 (2008)2026

Class I (1 since 2007) Class II/III not classified

Adverse event reports per year · DPS

55in 2025

2007high 121 (2011) · low 9 (2007)2025

MAUDE reports naming product code DPS, not matched to any one device; reports are not rates.

View these four charts as a table

Year	Decisions	Median 510(k) review, days	Recalls (Class I)	MAUDE reports
2007	11	87	2	9
2008	13	31	0	17
2009	14	84	1	14
2010	11	104	2	21
2011	22	154	1	121
2012	12	117	0	56
2013	10	134	0	15
2014	11	253	0	15
2015	8	178	0	30
2016	11	229	0	12
2017	9	177	0	15
2018	14	221	0	19
2019	3	178	9	27
2020	6	224	2	59
2021	5	135	1	24
2022	6	244	1	59
2023	10	236	3	54
2024	8	260	4 (1)	64
2025	6	163	3	55
2026	6	258	4	—

What is it indicated for?

To power the functions of various devices for which batteries or battery packs are configured.

Since rechargeable batteries and battery packs are “device specific” and are designed to operate and fit into the equipment

for which they were manufactured only qualified personnel should evaluate, test, charge, or install these devices.

Battery Packs are is shipped only to customers who request a replacement battery for a particular device or to replace a

competitor’s battery. The biomedical equipment technician therefore knows the intended use is as a replacement battery.

Indications for use as stated in the FDA summary.

https://510kreport.com/device/K160667 · printed Nov 6, 2026

Cite this page

510(k) Report. “K160667: Anybattery C2 Rechargeable Battery.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K160667

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Record history

FDA decision record loaded May 2, 2026
Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
Lineage and recalls computed Nov 3, 2026
Page last updated Nov 3, 2026