Cleared Traditional

K902690 - SONICAID MODEL MERIDIAN 800

K902690 is an FDA 510(k) clearance for SONICAID MODEL MERIDIAN 800, manufactured by Oxford Medilog, Inc.. The device is a Class 2 Obstetrics & Gynecology device with product code HGM cleared through the Traditional 510(k) pathway after a 231-day FDA review.

K902690 · Oxford Medilog, Inc. · Obstetrics & Gynecology device
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Feb 1991
Decision
231d
Days
Class 2
Risk

K902690 is an FDA 510(k) clearance for the SONICAID MODEL MERIDIAN 800. Classified as System, Monitoring, Perinatal (product code HGM), Class II - Special Controls.

Submitted by Oxford Medilog, Inc. (Clearwater, US). The FDA issued a Cleared decision on February 5, 1991 after a review of 231 days - an extended review 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: 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 Oxford Medilog, Inc. devices

FDA 510(k) Submission Details - K902690

510(k) Number K902690 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 19, 1990
Decision Date February 05, 1991
Days to Decision 231 days
Submission Type Traditional
Review Panel Obstetrics & Gynecology (OB)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
71d slower than avg
Panel avg: 160d · This submission: 231d
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 97
Devices cleared under the same product code (HGM) and FDA review panel - the closest regulatory comparables to K902690.
LIFE-TRACE DISPOSABLE LEG PLATE PRODUCT # LT-100
K910418 · Graphic Controls Corp. · Jul 1991
COROMETRICS MDL 330 FETAL/MATERNAL TELEMETRY SYST
K910260 · Ge Medical Systems Information Technologies · Mar 1991
CATALOG NUMBER 2609 LEG PLATE
K905295 · Ge Medical Systems Information Technologies · Feb 1991
MODEL 855 ENHANCED PERFORMANCE REMOTE TERMINAL
K904358 · Ge Medical Systems Information Technologies · Oct 1990
M1350A FETAL MONITOR (INTRAPARTUM)
K900480 · Hewlett-Packard Co. · Jul 1990
MODEL 410T TELECOMMUNICATION SYSTEM
K895045 · Ge Medical Systems Information Technologies · Nov 1989