PREVENA 125 and PREVENA PLUS 125 Therapy Units— 510(k) DEN180013

Unknown

Kci USA, Inc.

FDA 510(k) clearance DEN180013 for PREVENA 125 and PREVENA PLUS 125 Therapy Units, Unknown on 2019-04-19. Applicant: Kci USA, Inc..

Clearance details

Applicant: Kci USA, Inc.
Product code: Code QFC
Advisory panel: General, Plastic Surgery
Date received: 2018-03-15
Decision date: 2019-04-19
Decision: Unknown
Clearance type: Direct
Location: San Antonio, TX, US

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