meddevicedb.com FDA Device Reference

DRESSING CHANGE KIT

K760912 Class I Traditional
Decision Date
1976-12-02
Sponsor / Applicant
American Hospital Supply Corp.

Technical Specification

510(k) Submission ID K760912
Product Code KGO
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4460
Decision Date 1976-12-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DRESSING CHANGE KIT received FDA 510(k) clearance under submission number K760912, sponsored by American Hospital Supply 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 1976-12-02.

Classification & Regulation

This clearance is catalogued under FDA product code KGO and 21 CFR 878.4460, within the General, Plastic Surgery review panel as a Class I device.