meddevicedb.com FDA Device Reference

MODIFICATION TO CONVERTORS SURGICAL GOWNS

K001189 Class II Special
Decision Date
2000-04-21
Sponsor / Applicant
Allegiance Healthcare Corp.

Technical Specification

510(k) Submission ID K001189
Product Code FYA
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4040
Decision Date 2000-04-21
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODIFICATION TO CONVERTORS SURGICAL GOWNS received FDA 510(k) clearance under submission number K001189, sponsored by Allegiance Healthcare Corp.. The device was reviewed via the Special premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2000-04-21.

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.