510(k) Report

510(k) · Cleared

Cleared

TigerConnect Alarm Management

K243270510(k) TraditionalCleared Sep 30, 2025349-day reviewClass II21 CFR 870.2300

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

Tigerconnect · MSX System, Network And Communication, Physiological Monitors

Cleared on Sep 30, 2025 as substantially equivalent to K193043 (Critical Alert, 2020) and 1 other predicate after a 349-day review. Its family tree reaches back 8 generations to 1997.

Decided
Sep 30, 2025
Review
349 days
Class
Class II
Product code
MSX
Recalls
None
Predicates
2

Its longest line of descent runs back 8 generations to K962827 (1997). 12 ancestors in all, the oldest K945277 (1995). No later device cites it as a predicate yet.

  1. Root · 8 generations backK962827 Alarm Display Unit/Pager-Lan System (Adu)Marquette Electronics, Inc. · 1997
  2. 7 generations backK971868 Impact (Informing Mobile Personnel and Care Tracking) Pager SystemMarquette Electronics, Inc. · 1997
  3. 6 generations backK973527 Cardio-Pager SystemData Critical Corp. · 1998
  4. 5 generations backK992749 Ultraview Waveform Pager System, Model 91841Spacelabs Medical, Inc. · 2000
  5. 4 generations backK062278 Spacelabs Medical Clinical Event Interface, Model 91847Spacelabs Medical, Inc. · 2006
  6. 3 generations backK103634 Ascom Clinicalconnex CardiomaxAscom (Us), Inc. · 2011
  7. 2 generations backK180566 Unite Connect for Clinical SystemsAscom Sweden AB · 2018
  8. 1 generation backK193043 Critical Alert CommonPath EnterpriseCritical Alert · 2020
  9. This deviceK243270 TigerConnect Alarm ManagementTigerconnect · 2025
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−8K962827Alarm Display Unit/Pager-Lan System (Adu)Marquette Electronics, Inc.1997—
−7K971868Impact (Informing Mobile Personnel and Care Tracking) Pager SystemMarquette Electronics, Inc.1997—
−6K973527Cardio-Pager SystemData Critical Corp.1998—
−5K992749Ultraview Waveform Pager System, Model 91841Spacelabs Medical, Inc.2000—
−4K062278Spacelabs Medical Clinical Event Interface, Model 91847Spacelabs Medical, Inc.2006—
−3K103634Ascom Clinicalconnex CardiomaxAscom (Us), Inc.2011—
−2K180566Unite Connect for Clinical SystemsAscom Sweden AB2018—
−1K193043Critical Alert CommonPath EnterpriseCritical Alert2020—
0 (this device)K243270TigerConnect Alarm ManagementTigerconnect2025—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199510
201110
201310
202010
FIG. 1 — Lineage of K243270, 1997–2025Source: 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 MSX? 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 MSX device

  1. #1 K242750 Central Stationscore 21.5 · 31 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) Report

What was it cleared against? (2)

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
*K193043Critical Alert CommonPath Enterprise
Summary page 6
…e Manufacturer / Model Equivalent Devices: TigerConnect 510(k) Model Number TigerConnect K193043 Critical Alert / Critical Alert CommonPath Alarm (Primary Predica…
Critical Alert2020—
*K193421Smart Alarm Interface
Summary page 6
…monPath Alarm (Primary Predicate) Management K193421 BoxView, LLC / BoxView Smart Alarm Interface (SAI), Model S…
Boxview, LLC2020—

What descends from it?

No later submission names this one as a predicate yet.

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 28 years and passes through 7 companies; a new generation was cleared every 4.4 years on median.
  • 1 of the 12 ancestors has a recall of any class.

How does its category compare?

All MSX devices

MSX System, Network And Communication, Physiological Monitors: FDA decisions, review times, recalls and adverse event reports over 20 years. 2025, this device’s year, is highlighted.

FDA decisions per year · MSX

4in 2025

2007: 42008: 12009: 12010: 32011: 72012: 42013: 22014: 32015: 52016: 32017: 22018: 42019: 42020: 52021: 32022: 52023: 32024: 42025: 42026 (partial year): 5
2007high 7 (2011) · low 1 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MSX

295in 2025

2007: 58 days median2010: 43 days median2011: 72 days median2012: 145 days median2014: 165 days median2015: 138 days median2016: 174 days median2018: 111 days median2019: 92 days median2020: 193 days median2021: 227 days median2022: 177 days median2023: 244 days median2024: 212 days median2025: 295 days median2026 (partial year): 145 days median
2007high 295 (2025) · low 43 (2010)2026

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

Recalls per year · MSX

1in 2025

2007: 12008: 12009: 22010: 12011: 12012: 22015: 22017: 22018: 12022: 12025: 12026 (partial year): 2
2007high 2 (2009) · low 0 (2013)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · MSX

19in 2025

2007: 52008: 62009: 72010: 142011: 32012: 42013: 172014: 322015: 312016: 112017: 162018: 152019: 152020: 252021: 172022: 182023: 102024: 322025: 19
2007high 32 (2014) · low 3 (2011)2025

MAUDE reports naming product code MSX, 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
200745815
20081—16
20091—27
2010343114
201177213
2012414524
20132—017
20143165032
20155138231
20163174011
20172—216
20184111115
2019492015
20205193025
20213227017
20225177118
20233244010
20244212032
20254295119
202651452—

What is it indicated for?

The intended use of TigerConnect Alarm Management is to provide an interface with clinical systems to forward information associated to the particular event to the designated display device(s). For medical alarms, TigerConnect Alarm Management is intended to serve as a parallel, redundant, forwarding mechanism to inform healthcare professionals of particular medical related events TigerConnect Alarm Management does not alter the behavior of the primary…

Read the full statement (108 words)

The intended use of TigerConnect Alarm Management is to provide an interface with clinical systems to forward information associated to the particular event to the designated display device(s).

For medical alarms, TigerConnect Alarm Management is intended to serve as a parallel, redundant, forwarding mechanism to inform healthcare professionals of particular medical related events TigerConnect Alarm Management does not alter the behavior of the primary medical devices and associated alarm annunciations. The display device provides a visual, and/or audible and/or vibrating mechanism upon receipt of the alert.

TigerConnect Alarm Management is intended for use as a secondary alert. It does not replace the alarm function on the primary device.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K243270: TigerConnect Alarm Management.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K243270

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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