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NON-STICK BIPOLAR FORCEPS

K992931 Class II Traditional
Decision Date
1999-11-17
Sponsor / Applicant
Silverglide Surgical Technologies

Technical Specification

510(k) Submission ID K992931
Product Code GEI
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4400
Decision Date 1999-11-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NON-STICK BIPOLAR FORCEPS received FDA 510(k) clearance under submission number K992931, sponsored by Silverglide Surgical Technologies. 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 1999-11-17.

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.