REHASTIM 2, REHAMOVE 2— 510(k) K112844

Substantially Equivalent

Hasomed GmbH

FDA 510(k) clearance K112844 for REHASTIM 2, REHAMOVE 2, Substantially Equivalent on 2011-10-27. Applicant: Hasomed GmbH. Device class: 2.

Clearance details

Applicant: Hasomed GmbH
Product code: Code GZI
Device class: Class 2
Regulation: 21 CFR 882.5810
Advisory panel: Neurology
Date received: 2011-09-29
Decision date: 2011-10-27
Decision: Substantially Equivalent
Clearance type: Special
Location: Magdeburg, 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.