510(k) Report

510(k) · Cleared

Cleared

Pulseco Hemodynamic Monitor CM71

K010049510(k) TraditionalCleared Jun 14, 2001160-day reviewClass II21 CFR 870.1435

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

Lidco, Ltd. · DXG Computer, Diagnostic, Pre-Programmed, Single-Function

Cleared on Jun 14, 2001 after a 160-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 1 later device descends from it.

Decided
Jun 14, 2001
Review
160 days
Class
Class II
Product code
DXG
Recalls
None
Predicates
0

1 later device descends from it, 1 citing it directly.

Descendants, by year cleared 2014: 1 descendant cleared200020052010201520202025
  1. This deviceK010049 Pulseco Hemodynamic Monitor CM71Lidco, Ltd. · 2001
  2. Descendant · cites it directly · 0 of its ownK134035 Transonic HCM 103 SystemTransonic Systems, Inc. · 2014

Most influential descendants

Showing 1 of 1 · See all
  • K134035Transonic HCM 103 SystemTransonic Systems, Inc. · 2014 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K010049Pulseco Hemodynamic Monitor CM71Lidco, Ltd.2001—
+1K134035Transonic HCM 103 SystemTransonic Systems, Inc.2014—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201410
FIG. 1 — Lineage of K010049, 2001–2014Source: 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 DXG? 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 DXG device

  1. #1 K253092 Argos Infinity (Rev. 1.0)score 11.2 · 2 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 has not posted a summary or statement for it, so its predicates are not known.

What descends from it? (1)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K134035Transonic HCM 103 SystemTransonic Systems, Inc.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?

  • Of its descendants, K134035 (Transonic Systems, Inc., 2014) has gone furthest, with 0 descendants of its own.

How does its category compare?

All DXG devices

DXG Computer, Diagnostic, Pre-Programmed, Single-Function: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · DXG

1in 2025

2007: 12008: 52010: 42011: 32012: 22013: 32014: 62015: 12016: 12017: 12018: 22019: 22020: 12021: 12023: 12025: 12026 (partial year): 1
2007high 6 (2014) · low 0 (2009)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · DXG

290in 2014

2008: 118 days median2010: 282 days median2011: 104 days median2013: 236 days median2014: 290 days median
2007high 290 (2014) · low 104 (2011)2026

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

Recalls per year · DXG

2in 2020

2007: 12008: 12009: 62010: 12020: 2
2007high 6 (2009) · low 0 (2011)2026

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

Adverse event reports per year · DXG

8in 2025

2007: 432008: 372009: 82010: 172011: 72012: 292013: 232014: 442015: 342016: 672017: 622018: 832019: 812020: 492021: 292022: 442023: 122024: 212025: 8
2007high 83 (2018) · low 7 (2011)2025

MAUDE reports naming product code DXG, 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
20071—143
20085118137
20090—68
20104282117
2011310407
20122—029
20133236023
20146290044
20151—034
20161—067
20171—062
20182—083
20192—081
20201—249
20211—029
20220—044
20231—012
20240—021
20251—08
20261—0—
Cite this page

510(k) Report. “K010049: Pulseco Hemodynamic Monitor CM71.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 3, 2026. https://510kreport.com/device/K010049

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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