meddevicedb.com FDA Device Reference

SURGICAL GOWNS AND DRAPES

K781099 Class II Traditional
Decision Date
1978-08-14
Sponsor / Applicant
Convertors

Technical Specification

510(k) Submission ID K781099
Product Code FYA
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4040
Decision Date 1978-08-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SURGICAL GOWNS AND DRAPES received FDA 510(k) clearance under submission number K781099, sponsored by Convertors. 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 1978-08-14.

Classification & Regulation

This clearance is catalogued under FDA product code FYA and 21 CFR 878.4040, within the General, Plastic Surgery review panel as a Class II device.