meddevicedb.com FDA Device Reference

GAUZE BANDAGE ROLL

K914842 Class I Traditional
Decision Date
1991-12-04
Sponsor / Applicant
Cal West Trading Co.

Technical Specification

510(k) Submission ID K914842
Product Code NAB
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4014
Decision Date 1991-12-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

GAUZE BANDAGE ROLL received FDA 510(k) clearance under submission number K914842, sponsored by Cal West Trading Co.. 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 1991-12-04.

Classification & Regulation

This clearance is catalogued under FDA product code NAB and 21 CFR 878.4014, within the General, Plastic Surgery review panel as a Class I device.