meddevicedb.com FDA Device Reference

BANDBAG, WRAP, STERILE

K820692 Class II Traditional
Decision Date
1982-05-03
Sponsor / Applicant
Contour Fabricators, Inc.

Technical Specification

510(k) Submission ID K820692
Product Code MMP
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4370
Decision Date 1982-05-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BANDBAG, WRAP, STERILE received FDA 510(k) clearance under submission number K820692, sponsored by Contour Fabricators, 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 1982-05-03.

Classification & Regulation

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