Cleared Traditional

K991739 - COROMETRICS 120 SERIES MATERNAL/FETAL MONITOR

K991739 is an FDA 510(k) clearance for COROMETRICS 120 SERIES MATERNAL/FETAL M..., manufactured by General Electric Medical Systems Information Techn. The device is a Class 2 Obstetrics & Gynecology device with product code HGM cleared through the Traditional 510(k) pathway after a 90-day FDA review.

K991739 · General Electric Medical Systems Information Techn · Obstetrics & Gynecology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Aug 1999
Decision
90d
Days
Class 2
Risk

K991739 is an FDA 510(k) clearance for the COROMETRICS 120 SERIES MATERNAL/FETAL MONITOR. Classified as System, Monitoring, Perinatal (product code HGM), Class II - Special Controls.

Submitted by General Electric Medical Systems Information Techn (Annapolis, US). The FDA issued a Cleared decision on August 19, 1999 after a review of 90 days - within the typical 510(k) review window.

This device falls under the Obstetrics & Gynecology FDA review panel, regulated under 21 CFR 884.2740 - the FDA obstetrics and gynecology device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Obstetrics & Gynecology review framework, consistent with the majority of Class II 510(k) submissions.

View all General Electric Medical Systems Information Techn devices

FDA 510(k) Submission Details - K991739

510(k) Number K991739 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 21, 1999
Decision Date August 19, 1999
Days to Decision 90 days
Submission Type Traditional
Review Panel Obstetrics & Gynecology (OB)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
70d faster than avg
Panel avg: 160d · This submission: 90d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

HGM Device Classification - Class 2, Special Controls

Product Code HGM System, Monitoring, Perinatal
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 884.2740
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Obstetrics & Gynecology devices follow this clearance model.

Regulatory Peers - HGM System, Monitoring, Perinatal

All 162
Devices cleared under the same product code (HGM) and FDA review panel - the closest regulatory comparables to K991739.
BABY DOPPLEX 4000, MODEL BD 4000
K990569 · Huntleigh Healthcare, Inc. · Jan 2000
QUANTITATIVE SENTINEL SYSTEM
K993008 · Marquette Medical Systems, Inc. · Dec 1999
COROMETRICS MODEL 171 AND 172 FETAL MONITOR
K991905 · General Electric Medical Systems Information Techn · Sep 1999
FETALGARD 3000 FETAL MONITOR
K983395 · Analogic Corp. · Aug 1999
WATCHCHILD OBSTERICAL PATIENT DATA MANAGEMENT SYSTEM
K974248 · Air-Shields, Inc. · Oct 1998
CALM
K980719 · Lms Medical Systems , Ltd. · Jul 1998