Dermapose Access— 510(k) K200168
Substantially EquivalentPuregraft, LLC
FDA 510(k) clearance K200168 for Dermapose Access, Substantially Equivalent on 2020-04-22. Applicant: Puregraft, LLC. Device class: 2.
Clearance details
- Applicant
- Puregraft, LLC
- Product code
- Code QPB
- Device class
- Class 2
- Regulation
- 21 CFR 878.5040
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Solana Beach, CA, US
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