MICRODERM, MODEL/VERSION 3.5— 510(k) K040171

Substantially Equivalent

Visiomed AG

FDA 510(k) clearance K040171 for MICRODERM, MODEL/VERSION 3.5, Substantially Equivalent on 2004-06-08. Applicant: Visiomed AG. Device class: 2.

Clearance details

Applicant: Visiomed AG
Product code: Code PSN
Device class: Class 2
Regulation: 21 CFR 878.4580
Advisory panel: General, Plastic Surgery
Date received: 2004-01-26
Decision date: 2004-06-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: South West Ranches, FL, 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.