meddevicedb.com FDA Device Reference

VARIOUS SURG. & DIAGNOSTIC INSTRU. ETC.

K770428 Class I Traditional
Decision Date
1979-09-12
Sponsor / Applicant
Holco Instrument Corp.

Technical Specification

510(k) Submission ID K770428
Product Code FSM
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4800
Decision Date 1979-09-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VARIOUS SURG. & DIAGNOSTIC INSTRU. ETC. received FDA 510(k) clearance under submission number K770428, sponsored by Holco Instrument 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 1979-09-12.

Classification & Regulation

This clearance is catalogued under FDA product code FSM and 21 CFR 878.4800, within the General, Plastic Surgery review panel as a Class I device.