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MALIS CMC-II BIPOLAR COAGULATOR & CUT

K831508 Class II Traditional
Decision Date
1983-06-24
Sponsor / Applicant
Valley Forge Scientific Corp.

Technical Specification

510(k) Submission ID K831508
Product Code GEI
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4400
Decision Date 1983-06-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MALIS CMC-II BIPOLAR COAGULATOR & CUT received FDA 510(k) clearance under submission number K831508, sponsored by Valley Forge Scientific 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 1983-06-24.

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.