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BIPOLAR SUCTION COAGULATOR

K965241 Class II Traditional
Decision Date
1997-02-28
Sponsor / Applicant
Kirwan Surgical Products, Inc.

Technical Specification

510(k) Submission ID K965241
Product Code GEI
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4400
Decision Date 1997-02-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BIPOLAR SUCTION COAGULATOR received FDA 510(k) clearance under submission number K965241, sponsored by Kirwan Surgical Products, 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 1997-02-28.

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.