510(k) Report

510(k) · Cleared

Cleared

Fetal Ultrasonic Monitor and Accessories

K131457510(k) TraditionalCleared Jan 24, 2014249-day reviewClass II21 CFR 884.2660

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

Shenzhen Jumper Medical Equipment Co., Ltd. · KNG Monitor, Ultrasonic, Fetal

Cleared on Jan 24, 2014 as substantially equivalent to K112911 (Beijing Choice Electronic Technololgy Co., Ltd., 2011) after a 249-day review. Its family tree reaches back 6 generations to 1994. 6 later devices descend from it.

Decided
Jan 24, 2014
Review
249 days
Class
Class II
Product code
KNG
Recalls
None
Predicates
1

Its longest line of descent runs back 6 generations to K930200 (1994). 6 later devices descend from it, 2 citing it directly.

  1. Root · 6 generations backK930200 Multi Dopplex II / Fetal Dopplex IIHuntleigh Healthcare, Inc. · 1994
  2. 5 generations backK991441 Cadence Doppler Ultrasound SystemMedasonics, Inc. · 1999
  3. 4 generations backK024197 Lifedop DopplerSummit Doppler Systems, Inc. · 2003 · Recalled
  4. 3 generations backK082480 Contec Pocket Fetal DopplerContec Medical System Co., Ltd. · 2009
  5. 2 generations backK100626 Doppler Fetal Heart Rate Detector, Model FM-200Shenzhen Biocare Electronics Co., Ltd. · 2010
  6. 1 generation backK112911 Fetal DopplerBeijing Choice Electronic Technololgy Co., Ltd. · 2011
  7. This deviceK131457 Fetal Ultrasonic Monitor and AccessoriesShenzhen Jumper Medical Equipment Co., Ltd. · 2014
  8. Descendant · cites it directly · 4 of its ownK182526 Fetal Doppler (Models: FD-231B, FD-231D, FD-640B, FD-640D, FD-200B…Vcomin Technology Limited · 2019
  9. Descendant · 2 generations on · 1 of its ownK220245 Pocket Fetal Doppler (Models CONTEC10C and CONTEC10CL)Contec Medical Systems Co.,Ltd · 2022
  10. Descendant · 2 generations on · 1 of its ownK211940 Fetal DopplerShenzhen Taikang Medical Equipment Co., Ltd. · 2022
  11. Descendant · 3 generations on · 0 of its ownK252669 Fetal Doppler U8-25, U9-25Zhongshan Xiaolan Town Senlan Electronic Factory · 2026
  12. Descendant · 3 generations on · 0 of its ownK232893 Pocket Fetal Doppler (CONTEC 10D), Pocket Fetal Doppler (CONTEC…Contec Medical Systems Co.,Ltd · 2024

Showing 5 of 6 descendants. See all descendants

Descendants cleared per year

2018: 12019: 12022: 22024: 12026: 1
2018high 2 (2022) · low 0 (2020)2026

Most influential descendants

Showing 5 of 6 · See all
  • K182526Fetal Doppler (Models: FD-231B, FD-231D, FD-640B, FD-640D, FD-200B, FD-200D, FD-591B…Vcomin Technology Limited · 2019 · cites it directly4descendants
  • K220245Pocket Fetal Doppler (Models CONTEC10C and CONTEC10CL)Contec Medical Systems Co.,Ltd · 2022 · 2 generations on1descendant
  • K211940Fetal DopplerShenzhen Taikang Medical Equipment Co., Ltd. · 2022 · 2 generations on1descendant
  • K252669Fetal Doppler U8-25, U9-25Zhongshan Xiaolan Town Senlan Electronic Factory · 2026 · 3 generations on0descendants
  • K232893Pocket Fetal Doppler (CONTEC 10D), Pocket Fetal Doppler (CONTEC 10E), Pocket Fetal…Contec Medical Systems Co.,Ltd · 2024 · 3 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−6K930200Multi Dopplex II / Fetal Dopplex IIHuntleigh Healthcare, Inc.1994—
−5K991441Cadence Doppler Ultrasound SystemMedasonics, Inc.1999—
−4K024197Lifedop DopplerSummit Doppler Systems, Inc.20031
−3K082480Contec Pocket Fetal DopplerContec Medical System Co., Ltd.2009—
−2K100626Doppler Fetal Heart Rate Detector, Model FM-200Shenzhen Biocare Electronics Co., Ltd.2010—
−1K112911Fetal DopplerBeijing Choice Electronic Technololgy Co., Ltd.2011—
0 (this device)K131457Fetal Ultrasonic Monitor and AccessoriesShenzhen Jumper Medical Equipment Co., Ltd.2014—
+1K182526Fetal Doppler (Models: FD-231B, FD-231D, FD-640B, FD-640D, FD-200B, FD-200D…Vcomin Technology Limited2019—
+2K220245Pocket Fetal Doppler (Models CONTEC10C and CONTEC10CL)Contec Medical Systems Co.,Ltd2022—
+2K211940Fetal DopplerShenzhen Taikang Medical Equipment Co., Ltd.2022—
+3K252669Fetal Doppler U8-25, U9-25Zhongshan Xiaolan Town Senlan Electronic Factory2026—
+3K232893Pocket Fetal Doppler (CONTEC 10D), Pocket Fetal Doppler (CONTEC 10E), Pocket…Contec Medical Systems Co.,Ltd2024—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201810
201910
202220
202410
202610
FIG. 1 — Lineage of K131457, 1994–2026Source: 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 KNG? 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 KNG device

  1. #1 K252669 Fetal Doppler U8-25, U9-25score 13.0 · 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? (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
*K112911Fetal Doppler
Summary page 2
…660 5.3 Predicate Device Information Sponsor: Beijing Choice Electronic Technology Co., Ltd. Device: Fetal Doppler MD800 510(K) Number: K112911 5.4 Device Description JPD-1 008 Fetal Doppler is device prescribed by a licensed physician for use in hospitals and the homecar…
Beijing Choice Electronic Technololgy Co., Ltd.2011—
†K110124Fetal Doppler JPD-100SShenzhen Jumper Medical Equipment Co., Ltd.2011—

Also cleared against K112911: 1 other device →

What descends from it? (6)

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

NumberDeviceApplicantDecidedDescendants
K182526Fetal Doppler (Models: FD-231B, FD-231D, FD-640B, FD-640D, FD-200B, FD-200D, FD-591B…Vcomin Technology Limited20194
K172780SD1 Ultrasonic Pocket DopplerEdan Instruments, Inc.20180

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 20 years and passes through 7 companies; a new generation was cleared every 3.0 years on median.
  • 1 of the 6 ancestors has a recall of any class.
  • Of its descendants, K182526 (Vcomin Technology Limited, 2019) has gone furthest, with 4 descendants of its own.
  • 1 other device also cites its predicate K112911.

How does its category compare?

All KNG devices

KNG Monitor, Ultrasonic, Fetal: FDA decisions, review times, recalls and adverse event reports over 20 years. 2014, this device’s year, is highlighted.

FDA decisions per year · KNG

1in 2025

2008: 12009: 32010: 22011: 52014: 12015: 12016: 12018: 32019: 32021: 12022: 22024: 22025: 12026 (partial year): 1
2007high 5 (2011) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · KNG

202in 2019

2009: 181 days median2011: 57 days median2018: 154 days median2019: 202 days median
2007high 202 (2019) · low 57 (2011)2026

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

Recalls per year · KNG

No recall names KNG since 2007.

Adverse event reports per year · KNG

1in 2025

2008: 22013: 12014: 12017: 32018: 82019: 12020: 22021: 12023: 22024: 32025: 1
2007high 8 (2018) · low 0 (2007)2025

MAUDE reports naming product code KNG, 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
20070—00
20081—02
2009318100
20102—00
201155700
20120—00
20130—01
20141—01
20151—00
20161—00
20170—03
2018315408
2019320201
20200—02
20211—01
20222—00
20230—02
20242—03
20251—01
20261—0—

What is it indicated for?

The Fetal Doppler JPD-100B3 is a hand-held, battery powered audio Doppler device used for detecting fetal heart beats.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K131457: Fetal Ultrasonic Monitor and Accessories.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K131457

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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