Activmotion S
K-Number: K241539 · 2024-07-30
ApplicantNewclip Technics
Decision Date2024-07-30
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Activmotion S is a medical device manufactured by Newclip Technics. It received FDA 510(k) clearance on 2024-07-30 under approval number K241539. 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 S?
Activmotion S is a medical device that received FDA 510(k) clearance on 2024-07-30. It is manufactured by Newclip Technics. The 510(k) number is K241539.
When was Activmotion S approved by the FDA?
Activmotion S received FDA 510(k) clearance on 2024-07-30, under approval number K241539.
What company makes Activmotion S?
Activmotion S is manufactured by Newclip Technics.
What is the FDA product code for Activmotion S?
The FDA product code for Activmotion S 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.