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ACTIVAC THERAPY UNIT AND INFOVAC THERAPY UNIT, VAC ATS THERAPY UNIT AND VAC FREEDOM THERAPY UNIT, VAC VIA THERAPY UNIT

K120033 Class II Traditional
Decision Date
2012-05-31
Sponsor / Applicant
Kci USA, Inc.

Technical Specification

510(k) Submission ID K120033
Product Code OMP
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4780
Decision Date 2012-05-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ACTIVAC THERAPY UNIT AND INFOVAC THERAPY UNIT, VAC ATS THERAPY UNIT AND VAC FREEDOM THERAPY UNIT, VAC VIA THERAPY UNIT received FDA 510(k) clearance under submission number K120033, sponsored by Kci USA, Inc.. 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 2012-05-31.

Classification & Regulation

This clearance is catalogued under FDA product code OMP and 21 CFR 878.4780, within the General, Plastic Surgery review panel as a Class II device.