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INSTRUMENT RACK FOR DAWSON-YUHL INSTR.

K760579 Class I Traditional
Decision Date
1976-11-02
Sponsor / Applicant
V. Mueller O.V. Baxter Healthcare Corp.

Technical Specification

510(k) Submission ID K760579
Product Code FSM
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4800
Decision Date 1976-11-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

INSTRUMENT RACK FOR DAWSON-YUHL INSTR. received FDA 510(k) clearance under submission number K760579, sponsored by V. Mueller O.V. Baxter Healthcare Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1976-11-02.

Classification & Regulation

This clearance is catalogued under FDA product code FSM and 21 CFR 878.4800, within the General, Plastic Surgery review panel as a Class I device.