DP4 Microneedling device— 510(k) K221070

Substantially Equivalent

Equipmed USA, LLC

FDA 510(k) clearance K221070 for DP4 Microneedling device, Substantially Equivalent on 2022-12-20. Applicant: Equipmed USA, LLC.

Clearance details

Applicant: Equipmed USA, LLC
Product code: Code QAI
Advisory panel: General, Plastic Surgery
Date received: 2022-04-12
Decision date: 2022-12-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Newport Beach, CA, US

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