meddevicedb.com FDA Device Reference

CONVERTORS SMS DRAPES

K970554 Class II Traditional
Decision Date
1997-05-27
Sponsor / Applicant
Allegiance Healthcare Corp.

Technical Specification

510(k) Submission ID K970554
Product Code KKX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4370
Decision Date 1997-05-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CONVERTORS SMS DRAPES received FDA 510(k) clearance under submission number K970554, sponsored by Allegiance Healthcare 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 1997-05-27.

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.