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FLOW CONROL VALVE

K922781 Class II Traditional
Decision Date
1993-03-08
Sponsor / Applicant
American Omni Medical, Inc.

Technical Specification

510(k) Submission ID K922781
Product Code MJJ
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.4400
Decision Date 1993-03-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FLOW CONROL VALVE received FDA 510(k) clearance under submission number K922781, sponsored by American Omni Medical, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1993-03-08.

Classification & Regulation

This clearance is catalogued under FDA product code MJJ and 21 CFR 870.4400, within the Cardiovascular review panel as a Class II device.