510(k) Report

510(k) · Cleared

Cleared

TM2000 Fetaltrace Transtelephonic Receiving Center

K021574510(k) TraditionalCleared Aug 12, 200290-day reviewClass II21 CFR 884.2740

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

Card Guard Scientific Survival, Ltd. · HGM System, Monitoring, Perinatal

Cleared on Aug 12, 2002 as substantially equivalent to K013879 (Card Guard Scientific Survival, Ltd., 2002) after a 90-day review. Its family tree reaches back 2 generations to 1999.

Decided
Aug 12, 2002
Review
90 days
Class
Class II
Product code
HGM
Recalls
None
Predicates
1

Its longest line of descent runs back 2 generations to K992164 (1999). No later device cites it as a predicate yet.

  1. Root · 2 generations backK992164 Telemedicine 2000Card Guard Scientific Survival, Ltd. · 1999
  2. 1 generation backK013879 TM2000, Model 1Card Guard Scientific Survival, Ltd. · 2002
  3. This deviceK021574 TM2000 Fetaltrace Transtelephonic Receiving CenterCard Guard Scientific Survival, Ltd. · 2002
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K992164Telemedicine 2000Card Guard Scientific Survival, Ltd.1999—
−1K013879TM2000, Model 1Card Guard Scientific Survival, Ltd.2002—
0 (this device)K021574TM2000 Fetaltrace Transtelephonic Receiving CenterCard Guard Scientific Survival, Ltd.2002—
FIG. 1 — Lineage of K021574, 1999–2002Source: 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 HGM? 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 HGM device

  1. #1 K241882 Fetal & Maternal Monitor (F15A, F15A Air)score 19.5 · 33 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
*K013879TM2000, Model 1
Summary page 4
…13879 Receiving Center, cleared on Nov 23, 2001. The TM2000 FetalTrace has the FetaVMaternal service, with the user interface forms totally identical to those of TM2000 K013879. The TM2000 FetalTrace differs from the TM2000 KO13879 in two aspects: 1. Unlike the TM2000 KO1 3879, the TM2000 FetalTrace h…
Card Guard Scientific Survival, Ltd.2002—

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 3 years and passes through 1 company; a new generation was cleared every 2.4 years on median.
  • None of the 2 ancestors has a recall.

How does its category compare?

All HGM devices

HGM System, Monitoring, Perinatal: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · HGM

4in 2025

2007: 32008: 42009: 42010: 42011: 132012: 42013: 22014: 42015: 52016: 12017: 32018: 32020: 12022: 12023: 22024: 12025: 42026 (partial year): 2
2007high 13 (2011) · low 0 (2019)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · HGM

269in 2025

2007: 56 days median2008: 75 days median2009: 66 days median2010: 193 days median2011: 141 days median2012: 107 days median2014: 231 days median2015: 169 days median2017: 138 days median2018: 258 days median2025: 269 days median
2007high 269 (2025) · low 56 (2007)2026

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

Recalls per year · HGM

5in 2019

2008: 42009: 62013: 12014: 12019: 52026 (partial year): 2
2007high 6 (2009) · low 0 (2007)2026

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

Adverse event reports per year · HGM

99in 2025

2007: 352008: 172009: 422010: 642011: 832012: 442013: 162014: 302015: 442016: 172017: 272018: 302019: 412020: 192021: 712022: 872023: 692024: 1742025: 99
2007high 174 (2024) · low 16 (2013)2025

MAUDE reports naming product code HGM, 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
2007356035
2008475417
2009466642
20104193064
201113141083
20124107044
20132—116
20144231130
20155169044
20161—017
20173138027
20183258030
20190—541
20201—019
20210—071
20221—087
20232—069
20241—0174
20254269099
20262—2—

What is it indicated for?

The TM2000 FetalTrace Telemedicine Receiving Center is intended for supporting

transtelephonic monitoring of the Fetal/Maternal parameters of patients.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K021574: TM2000 Fetaltrace Transtelephonic Receiving Center.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K021574

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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