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BUR, SURGICAL, GENERAL & PLASTIC SURGERY

K933595 Class I Traditional
Decision Date
1994-03-16
Sponsor / Applicant
Omega Surgical Instruments, Inc.

Technical Specification

510(k) Submission ID K933595
Product Code GFA
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4820
Decision Date 1994-03-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BUR, SURGICAL, GENERAL & PLASTIC SURGERY received FDA 510(k) clearance under submission number K933595, sponsored by Omega Surgical Instruments, Inc.. 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 1994-03-16.

Classification & Regulation

This clearance is catalogued under FDA product code GFA and 21 CFR 878.4820, within the General, Plastic Surgery review panel as a Class I device.