RejuvatoneMD— 510(k) K152199
Substantially EquivalentTrophy Skin, Inc.
FDA 510(k) clearance K152199 for RejuvatoneMD, Substantially Equivalent on 2016-03-23. Applicant: Trophy Skin, Inc.. Device class: 2.
Clearance details
- Applicant
- Trophy Skin, Inc.
- Product code
- Code NFO
- Device class
- Class 2
- Regulation
- 21 CFR 882.5890
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Frisco, TX, US
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