Cleared Traditional

K790761 - FETASONDE MODEL 2108

K790761 is an FDA 510(k) clearance for FETASONDE MODEL 2108, manufactured by Roche Medical Electronics, Inc.. The device is a Class 2 Obstetrics & Gynecology device with product code HGM cleared through the Traditional 510(k) pathway after a 45-day FDA review.

K790761 · Roche Medical Electronics, Inc. · Obstetrics & Gynecology device
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Jun 1979
Decision
45d
Days
Class 2
Risk

K790761 is an FDA 510(k) clearance for the FETASONDE MODEL 2108. Classified as System, Monitoring, Perinatal (product code HGM), Class II - Special Controls.

Submitted by Roche Medical Electronics, Inc. (Mchenry, US). The FDA issued a Cleared decision on June 1, 1979 after a review of 45 days - a notably fast clearance cycle.

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: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Roche Medical Electronics, Inc. devices

FDA 510(k) Submission Details - K790761

510(k) Number K790761 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 17, 1979
Decision Date June 01, 1979
Days to Decision 45 days
Submission Type Traditional
Review Panel Obstetrics & Gynecology (OB)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
115d faster than avg
Panel avg: 160d · This submission: 45d
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 160
Devices cleared under the same product code (HGM) and FDA review panel - the closest regulatory comparables to K790761.
MODEL AP 180 MINI-MONITOR
K812256 · Sonicaid, Inc. · Oct 1981
TERUMO FETAL MONITOR # FHM-602
K801747 · Terumo Medical Corp. · Aug 1980
FETAL MONITOR MODEL FHM-1
K800013 · Advantage Medical Systems, Inc. · Mar 1980
MONITOR, OFFICE MODEL 140
K790139 · Ge Medical Systems Information Technologies · Feb 1979
MODEL 80032A, OBSTETRICAL TELEMETRY
K781359 · Hewlett-Packard Co. · Sep 1978
MODEL 80100A, PATIENT DATA MEMORY
K781360 · Hewlett-Packard Co. · Sep 1978