VariLymph 12 pro— 510(k) K193476

Substantially Equivalent

Slk Medical GmbH

FDA 510(k) clearance K193476 for VariLymph 12 pro, Substantially Equivalent on 2020-08-19. Applicant: Slk Medical GmbH. Device class: 2.

Clearance details

Applicant: Slk Medical GmbH
Product code: Code JOW
Device class: Class 2
Regulation: 21 CFR 870.5800
Advisory panel: Cardiovascular
Date received: 2019-12-16
Decision date: 2020-08-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Dortmund, DE

Download summary PDF View on FDA.gov ↗

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