Activmotion Range
K-Number: K173746 · 2018-02-27
ApplicantNewclip Technics
Decision Date2018-02-27
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Activmotion Range is a medical device manufactured by Newclip Technics. It received FDA 510(k) clearance on 2018-02-27 under approval number K173746. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Activmotion Range?
Activmotion Range is a medical device that received FDA 510(k) clearance on 2018-02-27. It is manufactured by Newclip Technics. The 510(k) number is K173746.
When was Activmotion Range approved by the FDA?
Activmotion Range received FDA 510(k) clearance on 2018-02-27, under approval number K173746.
What company makes Activmotion Range?
Activmotion Range is manufactured by Newclip Technics.
What is the FDA product code for Activmotion Range?
The FDA product code for Activmotion Range is HRS.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.