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CONMED/ASPEN LABS COATED LAPAROSCOPIC ELECTROSURGICAL BLADES

K952204 Class II Traditional
Decision Date
1995-05-25
Sponsor / Applicant
Conmedcorp

Technical Specification

510(k) Submission ID K952204
Product Code GEI
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4400
Decision Date 1995-05-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CONMED/ASPEN LABS COATED LAPAROSCOPIC ELECTROSURGICAL BLADES received FDA 510(k) clearance under submission number K952204, sponsored by Conmedcorp. 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 1995-05-25.

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.