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FDA 510(k)

RehaStim 2

K-Number: K162683 · 2017-02-03

ApplicantHasomed GmbH
Decision Date2017-02-03
Product CodeGZI
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

RehaStim 2 is a medical device manufactured by Hasomed GmbH. It received FDA 510(k) clearance on 2017-02-03 under approval number K162683. The device is classified under product code GZI. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RehaStim 2?

RehaStim 2 is a medical device that received FDA 510(k) clearance on 2017-02-03. It is manufactured by Hasomed GmbH. The 510(k) number is K162683.

When was RehaStim 2 approved by the FDA?

RehaStim 2 received FDA 510(k) clearance on 2017-02-03, under approval number K162683.

What company makes RehaStim 2?

RehaStim 2 is manufactured by Hasomed GmbH.

What is the FDA product code for RehaStim 2?

The FDA product code for RehaStim 2 is GZI.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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