510(k) Report

510(k) · Cleared

Cleared

Digital Electrocardiograph, Models Ecg-1210, Ecg-1230, Ecg-3010, Ecg-6010

K101876510(k) TraditionalCleared Mar 1, 2011238-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

Shenzhen Biocare Electronics Co., Ltd. · DPS Electrocardiograph

Cleared on Mar 1, 2011 as substantially equivalent to K091513 (Edan Instruments, Inc., 2009) after a 238-day review. Its family tree reaches back 5 generations to 1993. 13 later devices descend from it.

Decided
Mar 1, 2011
Review
238 days
Class
Class II
Product code
DPS
Recalls
None
Predicates
1

Its longest line of descent runs back 5 generations to K921669 (1993). 10 ancestors in all, the oldest K820885 (1982). 13 later devices descend from it, 4 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2000: 1 other ancestor1998: 1 other ancestor1989: 1 other ancestor1982: 1 other ancestor1994: 1 other ancestor2014: 3 descendants cleared2012: 2 descendants cleared2011: 1 descendant cleared2018: 2 descendants cleared2013: 2 descendants cleared2024: 1 descendant cleared2015: 2 descendants clearedK921669 · Marquette SL Series Transport Remote Acquisition · Marquette Electronics, Inc. · 1993K964750 · Eagle 4000 Patient Monitor · Marquette Electronics, Inc. · 1997K991735 · Mac Series Electrocardiographs Including Mac 5000, Mac PC, Mac 6, Mac VU, Mac 8 Electrocardiographs · General Electric Medical Systems Information Techn · 1999K014108 · Mac 5000 Ecg Analysis System · General Electric Medical Systems Information Techn · 2002K091513 · Smart Ecg Series Electrocardiograph, Models SE-3, SE-300A and 300B, SE-6, SE-600, SE-12, SE-12 Express and SE-1200 · Edan Instruments, Inc. · 2009 · recalled19801990200020102020
  1. Root · 5 generations backK921669 Marquette SL Series Transport Remote AcquisitionMarquette Electronics, Inc. · 1993
  2. 4 generations backK964750 Eagle 4000 Patient MonitorMarquette Electronics, Inc. · 1997
  3. 3 generations backK991735 Mac Series Electrocardiographs Including Mac 5000, Mac PC, Mac 6…General Electric Medical Systems Information Techn · 1999
  4. 2 generations backK014108 Mac 5000 Ecg Analysis SystemGeneral Electric Medical Systems Information Techn · 2002
  5. 1 generation backK091513 Smart Ecg Series Electrocardiograph, Models SE-3, SE-300A and 300B…Edan Instruments, Inc. · 2009 · Recalled
  6. This deviceK101876 Digital Electrocardiograph, Models Ecg-1210, Ecg-1230, Ecg-3010…Shenzhen Biocare Electronics Co., Ltd. · 2011
  7. Descendant · cites it directly · 9 of its ownK112431 Digital ElectrocardiographShenzhen Biocare Electronics Co., Ltd. · 2011
  8. Descendant · cites it directly · 8 of its ownK122712 Digital ElectrocardiographShenzhen Biocare Electronics Co., Ltd. · 2012
  9. Descendant · 2 generations on · 4 of its ownK123816 Digital ElectrocardiographsShenzhen Biocare Electronics Co., Ltd. · 2013
  10. Descendant · cites it directly · 3 of its ownK113485 ElectrocardiographShenzhen Carewell Electronics Co., Ltd. · 2012
  11. Descendant · 3 generations on · 1 of its ownK133985 Digital ElectrocardiographShenzhen Biocare Bio-Medical Equipment Co., Ltd. · 2015

Showing 5 of 13 descendants. See all descendants

Descendants cleared per year

2011: 12012: 22013: 22014: 32015: 22018: 22024: 1
2011high 3 (2014) · low 0 (2016)2026

Most influential descendants

Showing 5 of 13 · See all
  • K112431Digital ElectrocardiographShenzhen Biocare Electronics Co., Ltd. · 2011 · cites it directly9descendants
  • K122712Digital ElectrocardiographShenzhen Biocare Electronics Co., Ltd. · 2012 · cites it directly8descendants
  • K123816Digital ElectrocardiographsShenzhen Biocare Electronics Co., Ltd. · 2013 · 2 generations on4descendants
  • K113485ElectrocardiographShenzhen Carewell Electronics Co., Ltd. · 2012 · cites it directly3descendants
  • K133985Digital ElectrocardiographShenzhen Biocare Bio-Medical Equipment Co., Ltd. · 2015 · 3 generations on1descendant
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−5K921669Marquette SL Series Transport Remote AcquisitionMarquette Electronics, Inc.1993—
−4K964750Eagle 4000 Patient MonitorMarquette Electronics, Inc.1997—
−3K991735Mac Series Electrocardiographs Including Mac 5000, Mac PC, Mac 6, Mac VU, Mac…General Electric Medical Systems Information Techn1999—
−2K014108Mac 5000 Ecg Analysis SystemGeneral Electric Medical Systems Information Techn2002—
−1K091513Smart Ecg Series Electrocardiograph, Models SE-3, SE-300A and 300B, SE-6…Edan Instruments, Inc.20091
0 (this device)K101876Digital Electrocardiograph, Models Ecg-1210, Ecg-1230, Ecg-3010, Ecg-6010Shenzhen Biocare Electronics Co., Ltd.2011—
+1K112431Digital ElectrocardiographShenzhen Biocare Electronics Co., Ltd.2011—
+1K122712Digital ElectrocardiographShenzhen Biocare Electronics Co., Ltd.2012—
+2K123816Digital ElectrocardiographsShenzhen Biocare Electronics Co., Ltd.2013—
+1K113485ElectrocardiographShenzhen Carewell Electronics Co., Ltd.2012—
+3K133985Digital ElectrocardiographShenzhen Biocare Bio-Medical Equipment Co., Ltd.2015—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198210
198910
199410
199810
200010

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201110
201220
201320
201430
201520
201820
202410
FIG. 1 — Lineage of K101876, 1993–2024Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

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.

Planning a device in DPS? 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. #1 K212112 Cardiologs Holter Platformscore 18.6 · 5 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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What was it cleared against? (1)

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.

TypeNumberDeviceApplicantDecidedRecalls
*K091513Smart Ecg Series Electrocardiograph, Models SE-3, SE-300A and 300B, SE-6, SE-600, SE-12…
Summary page 1
…ign specifications and was substantially equivalent to the predicate device. Predicate Device Smart ECG (SE) Series Electrocardiograph, SE-12, K091513 SE Conclusion The proposed devices, Digital Electrocardiograph ECG-1210 / ECG-1230 / ECG-3010 / ECG-6010, are…
Edan Instruments, Inc.20091

Also cleared against K091513: 6 other devices →

What descends from it? (13)

See all 13

4 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K112431Digital ElectrocardiographShenzhen Biocare Electronics Co., Ltd.20119
K122712Digital ElectrocardiographShenzhen Biocare Electronics Co., Ltd.20128
K113485ElectrocardiographShenzhen Carewell Electronics Co., Ltd.20123
K131858Digital ElectrocardiographGuangdong Biolight Meditech Co., Ltd.20140

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • The line of descent spans 18 years and passes through 4 companies; a new generation was cleared every 2.5 years on median.
  • 1 of the 10 ancestors has a recall of any class.
  • Of its descendants, K112431 (Shenzhen Biocare Electronics Co., Ltd., 2011) has gone furthest, with 9 descendants of its own.
  • 6 other devices also cite its predicate K091513.

How does its category compare?

All DPS devices

DPS Electrocardiograph: FDA decisions, review times, recalls and adverse event reports over 20 years. 2011, this device’s year, is highlighted.

FDA decisions per year · DPS

6in 2025

2007: 112008: 132009: 142010: 112011: 222012: 122013: 102014: 112015: 82016: 112017: 92018: 142019: 32020: 62021: 52022: 62023: 102024: 82025: 62026 (partial year): 6
2007high 22 (2011) · low 3 (2019)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · DPS

163in 2025

2007: 87 days median2008: 31 days median2009: 84 days median2010: 104 days median2011: 154 days median2012: 117 days median2013: 134 days median2014: 253 days median2015: 178 days median2016: 229 days median2017: 177 days median2018: 221 days median2019: 178 days median2020: 224 days median2021: 135 days median2022: 244 days median2023: 236 days median2024: 260 days median2025: 163 days median2026 (partial year): 258 days median
2007high 260 (2024) · low 31 (2008)2026

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

Recalls per year · DPS

3in 2025

2007: 22009: 12010: 22011: 12019: 92020: 22021: 12022: 12023: 32024: 4, 1 Class I2025: 32026 (partial year): 4
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

2007: 92008: 172009: 142010: 212011: 1212012: 562013: 152014: 152015: 302016: 122017: 152018: 192019: 272020: 592021: 242022: 592023: 542024: 642025: 55
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
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
2007118729
20081331017
20091484114
201011104221
2011221541121
201212117056
201310134015
201411253015
20158178030
201611229012
20179177015
201814221019
20193178927
20206224259
20215135124
20226244159
202310236354
202482604 (1)64
20256163355
202662584—

What is it indicated for?

Digital Electrocardiographs, ECG-1210 / ECG-1230 / ECG-3010 / ECG-6010, are intended to acquire ECG signals from adult and pediatric patients through body surface ECG electrodes. The obtained ECG records can help users to analyze and diagnose heart disease. Digital Electrocardiographs shall be used in healthcare facilities by doctors and/or trained healthcare professionals.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K101876: Digital Electrocardiograph, Models Ecg-1210, Ecg-1230, Ecg-3010, Ecg-6010.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K101876

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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