Exceed Microneedling Device— 510(k) K180778

Substantially Equivalent

Mt. Derm GmbH

FDA 510(k) clearance K180778 for Exceed Microneedling Device, Substantially Equivalent on 2018-09-07. Applicant: Mt. Derm GmbH. Device class: 2.

Clearance details

Applicant: Mt. Derm GmbH
Product code: Code QAI
Device class: Class 2
Regulation: 21 CFR 878.4430
Advisory panel: General, Plastic Surgery
Date received: 2018-03-26
Decision date: 2018-09-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Berlin, DE

Download summary PDF View on FDA.gov ↗

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More clearances from Mt. Derm GmbH

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