510(k) Report

510(k) · Cleared

Cleared

Cardiomagic Software

K925639510(k) TraditionalCleared Jun 22, 1993225-day reviewClass II21 CFR 870.2920

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

Instromedix, Inc. · DXH Transmitters And Receivers, Electrocardiograph, Telephone

Cleared on Jun 22, 1993 after a 225-day review. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known. 2 later devices descend from it.

Decided
Jun 22, 1993
Review
225 days
Class
Class II
Product code
DXH
Recalls
None
Predicates
0

2 later devices descend from it, 2 citing it directly.

Descendants, by year cleared 1998: 1 descendant cleared1996: 1 descendant cleared1990200020102020
  1. This deviceK925639 Cardiomagic SoftwareInstromedix, Inc. · 1993
  2. Descendant · cites it directly · 1 of its ownK955891 Cardioview Transtelephonic SoftwareMicromedical, Inc. · 1996
  3. Descendant · cites it directly · 0 of its ownK981807 Cardiovision Software, Model S-CV5-96Shl Telemedicine International, Ltd. · 1998

Most influential descendants

Showing 2 of 2 · See all
  • K955891Cardioview Transtelephonic SoftwareMicromedical, Inc. · 1996 · cites it directly1descendant
  • K981807Cardiovision Software, Model S-CV5-96Shl Telemedicine International, Ltd. · 1998 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K925639Cardiomagic SoftwareInstromedix, Inc.1993—
+1K955891Cardioview Transtelephonic SoftwareMicromedical, Inc.1996—
+1K981807Cardiovision Software, Model S-CV5-96Shl Telemedicine International, Ltd.1998—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
199610
199810
FIG. 1 — Lineage of K925639, 1993–1998Source: 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), 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. #1 K243438 MEMO Patch M (MPT-E08R-UNC01)score 12.9 · 9 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?

FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

What descends from it? (2)

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

NumberDeviceApplicantDecidedDescendants
K955891Cardioview Transtelephonic SoftwareMicromedical, Inc.19961
K981807Cardiovision Software, Model S-CV5-96Shl Telemedicine International, Ltd.19980

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?

  • Of its descendants, K955891 (Micromedical, Inc., 1996) has gone furthest, with 1 descendant of its own.

How does its category compare?

All DXH devices

DXH Transmitters And Receivers, Electrocardiograph, Telephone: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · DXH

4in 2025

2007: 32008: 72009: 22010: 22012: 12013: 32014: 62015: 42016: 12017: 52018: 42019: 62020: 52021: 32022: 42023: 12025: 42026 (partial year): 1
2007high 7 (2008) · low 0 (2011)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · DXH

322in 2025

2007: 202 days median2008: 41 days median2013: 206 days median2014: 186 days median2015: 142 days median2017: 150 days median2018: 294 days median2019: 177 days median2020: 141 days median2021: 107 days median2022: 150 days median2025: 322 days median
2007high 322 (2025) · low 41 (2008)2026

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

Recalls per year · DXH

1in 2015

2008: 42011: 32015: 12026 (partial year): 1
2007high 4 (2008) · low 0 (2007)2026

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

Adverse event reports per year · DXH

27in 2025

2009: 12010: 42011: 12012: 12013: 12014: 12016: 52017: 42020: 52021: 22022: 62023: 42024: 22025: 27
2007high 27 (2025) · low 0 (2007)2025

MAUDE reports naming product code DXH, 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
2007320200
200874140
20092—01
20102—04
20110—31
20121—01
2013320601
2014618601
2015414210
20161—05
2017515004
2018429400
2019617700
2020514105
2021310702
2022415006
20231—04
20240—02
20254322027
20261—1—
Cite this page

510(k) Report. “K925639: Cardiomagic Software.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K925639

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Record history
  • FDA decision record loaded May 2, 2026
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026