PREVENA 125 and PREVENA PLUS 125 Therapy Units— 510(k) DEN180013
UnknownKci 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.. Device class: 2.
Clearance details
- Applicant
- Kci USA, Inc.
- Product code
- Code QFC
- Device class
- Class 2
- Regulation
- 21 CFR 878.4783
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Direct
- Location
- San Antonio, TX, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.