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ABACUS OB ULTRASOUNG COMPUTER SOFTWARE

K951393 Class II Traditional
Decision Date
1995-05-01
Sponsor / Applicant
Solomon Technology Labs

Technical Specification

510(k) Submission ID K951393
Product Code HEM
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.2225
Decision Date 1995-05-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ABACUS OB ULTRASOUNG COMPUTER SOFTWARE received FDA 510(k) clearance under submission number K951393, sponsored by Solomon Technology Labs. The device was reviewed via the Traditional premarket notification pathway and assigned to the Obstetrics/Gynecology review panel. The statutory decision date of record is 1995-05-01.

Classification & Regulation

This clearance is catalogued under FDA product code HEM and 21 CFR 884.2225, within the Obstetrics/Gynecology review panel as a Class II device.