Dermapose Refresh— 510(k) K193363

Substantially Equivalent

Puregraft, LLC

FDA 510(k) clearance K193363 for Dermapose Refresh, Substantially Equivalent on 2020-04-14. Applicant: Puregraft, LLC. Device class: 2.

Clearance details

Applicant: Puregraft, LLC
Product code: Code MUU
Device class: Class 2
Regulation: 21 CFR 878.5040
Advisory panel: General, Plastic Surgery
Date received: 2019-12-04
Decision date: 2020-04-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Solana Beach, CA, US

Download summary PDF View on FDA.gov ↗

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