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EVERSHEARS SCISSORS, BILAP PROBES, BICOAG FORCEPS

K955001 Class II Traditional
Decision Date
1995-12-13
Sponsor / Applicant
Everest Medical Corp.

Technical Specification

510(k) Submission ID K955001
Product Code GEI
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4400
Decision Date 1995-12-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EVERSHEARS SCISSORS, BILAP PROBES, BICOAG FORCEPS received FDA 510(k) clearance under submission number K955001, sponsored by Everest Medical 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 1995-12-13.

Classification & Regulation

This clearance is catalogued under FDA product code GEI and 21 CFR 878.4400, within the General, Plastic Surgery review panel as a Class II device.