meddevicedb.com FDA Device Reference

RESOLVE SURGICAL O.R. TOWELS

K001667 Class II Traditional
Decision Date
2000-06-23
Sponsor / Applicant
Allegiance Healthcare Corp.

Technical Specification

510(k) Submission ID K001667
Product Code KKX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4370
Decision Date 2000-06-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RESOLVE SURGICAL O.R. TOWELS received FDA 510(k) clearance under submission number K001667, 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 2000-06-23.

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.