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VOLMED OPERATION DRAPE

K955872 Class II Traditional
Decision Date
1996-03-12
Sponsor / Applicant
Medal Intl. Sales Co., LLC

Technical Specification

510(k) Submission ID K955872
Product Code KKX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4370
Decision Date 1996-03-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VOLMED OPERATION DRAPE received FDA 510(k) clearance under submission number K955872, sponsored by Medal Intl. Sales Co., LLC. 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 1996-03-12.

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.