meddevicedb.com FDA Device Reference

IMC SURGICAL DRAPE

K100991 Class II Traditional
Decision Date
2010-10-05
Sponsor / Applicant
International Medsurg Connection

Technical Specification

510(k) Submission ID K100991
Product Code KKX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4370
Decision Date 2010-10-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IMC SURGICAL DRAPE received FDA 510(k) clearance under submission number K100991, sponsored by International Medsurg Connection. 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 2010-10-05.

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.