meddevicedb.com FDA Device Reference

BARRIER O.B. PACK IV

K770560 Class II Traditional
Decision Date
1977-04-05
Sponsor / Applicant
Surgikos, Inc.

Technical Specification

510(k) Submission ID K770560
Product Code KKX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4370
Decision Date 1977-04-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BARRIER O.B. PACK IV received FDA 510(k) clearance under submission number K770560, sponsored by Surgikos, 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 1977-04-05.

Classification & Regulation

This clearance is catalogued under FDA product code KKX and 21 CFR 878.4370, within the General, Plastic Surgery review panel as a Class II device.