Dermapose Access— 510(k) K200168

Substantially Equivalent

Puregraft, LLC

FDA 510(k) clearance K200168 for Dermapose Access, Substantially Equivalent on 2020-04-22. Applicant: Puregraft, LLC.

Clearance details

Applicant: Puregraft, LLC
Product code: Code QPB
Advisory panel: General, Plastic Surgery
Date received: 2020-01-23
Decision date: 2020-04-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Solana Beach, CA, US

Download summary PDF View on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.