510(k) · Cleared
ClearedPhysioglove ET System
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Commwell R&D, Ltd. · DXH Transmitters And Receivers, Electrocardiograph, Telephone
Cleared on Aug 18, 2014 as substantially equivalent to K042254 (Card Guard Scientific Survival, Ltd., 2005) and 1 other predicate after a 258-day review. Its family tree reaches back 9 generations to 1993.
- Decided
- Aug 18, 2014
- Review
- 258 days
- Class
- Class II
- Product code
- DXH
- Recalls
- None
- Predicates
- 2
Its longest line of descent runs back 9 generations to K921669 (1993). 23 ancestors in all, the oldest K820885 (1982). No later device cites it as a predicate yet.
- Root · 9 generations backK921669 Marquette SL Series Transport Remote AcquisitionMarquette Electronics, Inc. · 1993
- 5 generations between
- 3 generations backK060833 12SL Ecg Analysis ProgramGe Medical Systems Information Technologies · 2006
- 2 generations backK092369 12SL Ecg Analysis ProgramGe Medical Systems Information Technologies · 2010
- 1 generation backK103791 Physioglove ES with Ecg AnalysisCommwell, Ltd. · 2011
- This deviceK133703 Physioglove ET SystemCommwell R&D, Ltd. · 2014
Show all 9 generations
- Root · 9 generations backK921669 Marquette SL Series Transport Remote AcquisitionMarquette Electronics, Inc. · 1993
- 8 generations backK964750 Eagle 4000 Patient MonitorMarquette Electronics, Inc. · 1997
- 7 generations backK991735 Mac Series Electrocardiographs Including Mac 5000, Mac PC, Mac 6…General Electric Medical Systems Information Techn · 1999
- 6 generations backK014108 Mac 5000 Ecg Analysis SystemGeneral Electric Medical Systems Information Techn · 2002
- 5 generations backK033492 Modification to Mac 5000 Ecg Analysis SystemGe Medical Systems Information Technologies · 2003
- 4 generations backK042177 Modification to Mac 5000 Ecg Analysis SystemGe Medical Systems Information Technologies · 2004
- 3 generations backK060833 12SL Ecg Analysis ProgramGe Medical Systems Information Technologies · 2006
- 2 generations backK092369 12SL Ecg Analysis ProgramGe Medical Systems Information Technologies · 2010
- 1 generation backK103791 Physioglove ES with Ecg AnalysisCommwell, Ltd. · 2011
- This deviceK133703 Physioglove ET SystemCommwell R&D, Ltd. · 2014
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −9 | K921669 | Marquette SL Series Transport Remote Acquisition | Marquette Electronics, Inc. | 1993 | — |
| −8 | K964750 | Eagle 4000 Patient Monitor | Marquette Electronics, Inc. | 1997 | — |
| −7 | K991735 | Mac Series Electrocardiographs Including Mac 5000, Mac PC, Mac 6, Mac VU, Mac… | General Electric Medical Systems Information Techn | 1999 | — |
| −6 | K014108 | Mac 5000 Ecg Analysis System | General Electric Medical Systems Information Techn | 2002 | — |
| −5 | K033492 | Modification to Mac 5000 Ecg Analysis System | Ge Medical Systems Information Technologies | 2003 | — |
| −4 | K042177 | Modification to Mac 5000 Ecg Analysis System | Ge Medical Systems Information Technologies | 2004 | — |
| −3 | K060833 | 12SL Ecg Analysis Program | Ge Medical Systems Information Technologies | 2006 | — |
| −2 | K092369 | 12SL Ecg Analysis Program | Ge Medical Systems Information Technologies | 2010 | — |
| −1 | K103791 | Physioglove ES with Ecg Analysis | Commwell, Ltd. | 2011 | — |
| 0 (this device) | K133703 | Physioglove ET System | Commwell R&D, Ltd. | 2014 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1982 | 1 | 0 |
| 1989 | 1 | 0 |
| 1994 | 1 | 0 |
| 1997 | 2 | 0 |
| 1998 | 3 | 0 |
| 2000 | 1 | 0 |
| 2001 | 2 | 0 |
| 2003 | 1 | 0 |
| 2005 | 1 | 0 |
| 2006 | 1 | 0 |
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 DXH? 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 DXH device
- #1 K243438 MEMO Patch M (MPT-E08R-UNC01)score 12.9 · 9 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the 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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K042254 | PMP4 Selfcheck EcgSummary page 5…70.2920 6.9 Panel Cardiovascular 6.10 Predicate Devices • PMP4 SelfCheck ECG [Card G u a r d Scientific Survival Ltd.] cleared under K042254 • PhysioGlove ES-1 with ECG Analysis Program [Commwell Ltd.] cleared under K103791 6.11 Intended Use / Indication… | 2005 |
| * | K103791 | Physioglove ES with Ecg AnalysisSummary page 5…[Card G u a r d Scientific Survival Ltd.] cleared under K042254 • PhysioGlove ES-1 with ECG Analysis Program [Commwell Ltd.] cleared under K103791 6.11 Intended Use / Indication for Use The PhysioGlove ET is intended for self-testing by patients and by healthcare profession… | 2011 |
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 21 years and passes through 5 companies; a new generation was cleared every 2.4 years on median.
- None of the 23 ancestors has a recall.
- 6 other devices also cite its predicate K042254.
How does its category compare?
All DXH devicesDXH Transmitters And Receivers, Electrocardiograph, Telephone: FDA decisions, review times, recalls and adverse event reports over 20 years. 2014, this device’s year, is highlighted.
FDA decisions per year · DXH
4in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · DXH
322in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · DXH
1in 2015
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · DXH
27in 2025
MAUDE reports naming product code DXH, 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 | 3 | 202 | 0 | 0 |
| 2008 | 7 | 41 | 4 | 0 |
| 2009 | 2 | — | 0 | 1 |
| 2010 | 2 | — | 0 | 4 |
| 2011 | 0 | — | 3 | 1 |
| 2012 | 1 | — | 0 | 1 |
| 2013 | 3 | 206 | 0 | 1 |
| 2014 | 6 | 186 | 0 | 1 |
| 2015 | 4 | 142 | 1 | 0 |
| 2016 | 1 | — | 0 | 5 |
| 2017 | 5 | 150 | 0 | 4 |
| 2018 | 4 | 294 | 0 | 0 |
| 2019 | 6 | 177 | 0 | 0 |
| 2020 | 5 | 141 | 0 | 5 |
| 2021 | 3 | 107 | 0 | 2 |
| 2022 | 4 | 150 | 0 | 6 |
| 2023 | 1 | — | 0 | 4 |
| 2024 | 0 | — | 0 | 2 |
| 2025 | 4 | 322 | 0 | 27 |
| 2026 | 1 | — | 1 | — |
What is it indicated for?
The PhysioGlove ET is intended for self-testing by patients and by health care professionals at home and at medical settings. This 12-lead electrocardiogram (ECG), allows remote patients to display and transmit their ECG data to medical professionals via a mobile platform (communication device) to a remote server. Specifically, the PhysioGlove ET is intended for patients who are concerned about their heart health and have the following problems that are…
Read the full statement (121 words)
The PhysioGlove ET is intended for self-testing by patients and by health care professionals at home and at medical settings. This 12-lead electrocardiogram (ECG), allows remote patients to display and transmit their ECG data to medical professionals via a mobile platform (communication device) to a remote server.
Specifically, the PhysioGlove ET is intended for patients who are concerned about their heart health and have the following problems that are suggestive of abnormal heart function:
The system only provides waveform parameters for healthcare provider interpretation and
does not provide suggested interpretations.
Skipped beats
Pounding heart (palpitations)
Heart racing or irregular pulse
Lightheadedness or faintness
Chest discomfort
Shortness of breath
High risk for heart problems
History of heart problems
Recipient of heart medications
Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.
https://510kreport.com/device/K133703 · printed Nov 6, 2026
Cite this page
510(k) Report. “K133703: Physioglove ET System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K133703
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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