meddevicedb.com FDA Device Reference

SURGICAL GOWNS, SHEETS

K781959 Class II Traditional
Decision Date
1979-01-10
Sponsor / Applicant
Convertors

Technical Specification

510(k) Submission ID K781959
Product Code KKX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4370
Decision Date 1979-01-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SURGICAL GOWNS, SHEETS received FDA 510(k) clearance under submission number K781959, 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 1979-01-10.

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.