V12 PRO— 510(k) K210913

Substantially Equivalent

Slk Medical GmbH

FDA 510(k) clearance K210913 for V12 PRO, Substantially Equivalent on 2021-08-04. Applicant: Slk Medical GmbH.

Clearance details

Applicant: Slk Medical GmbH
Product code: Code IRP
Advisory panel: Physical Medicine
Date received: 2021-03-29
Decision date: 2021-08-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Waltrop, DE

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