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FDA 510(k), K945062, VACPLUS
FDA 510(k), K945062, VACPLUS
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510(K) Number: K945062
Device Name: VACPLUS
Manufacturer: KINETIC CONCEPTS, INC.
Device Classification Name: Apparatus, Suction, Ward Use, Portable, Ac-Powered
Regulation Number: 878.4780
Classification Product Code: JCX
Date Received: 10/14/1994
Decision Date: 03/14/1995
Regulation Medical Specialty: General & Plastic Surgery
Device Name: VACPLUS
Manufacturer: KINETIC CONCEPTS, INC.
Device Classification Name: Apparatus, Suction, Ward Use, Portable, Ac-Powered
Regulation Number: 878.4780
Classification Product Code: JCX
Date Received: 10/14/1994
Decision Date: 03/14/1995
Regulation Medical Specialty: General & Plastic Surgery
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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