FDA 510(k)

Activmotion S DTO

K-Number: K202803 · 2021-12-16

Decision Date2021-12-16

Product CodeHRS

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

Activmotion S DTO is a medical device manufactured by Newclip Technics. It received FDA 510(k) clearance on 2021-12-16 under approval number K202803. 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 DTO?

Activmotion S DTO is a medical device that received FDA 510(k) clearance on 2021-12-16. It is manufactured by Newclip Technics. The 510(k) number is K202803.

When was Activmotion S DTO approved by the FDA?

Activmotion S DTO received FDA 510(k) clearance on 2021-12-16, under approval number K202803.

What company makes Activmotion S DTO?

Activmotion S DTO is manufactured by Newclip Technics.

What is the FDA product code for Activmotion S DTO?

The FDA product code for Activmotion S DTO 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.