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FDA 510(k)

Activmotion Range

K-Number: K173746 · 2018-02-27

Decision Date2018-02-27
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Activmotion Range is the device name listed in this FDA 510(k) record. The listed applicant is Newclip Technics. It received FDA 510(k) clearance on 2018-02-27 under 510(k) 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. The listed applicant is Newclip Technics. The 510(k) number is K173746.

When did Activmotion Range receive FDA 510(k) clearance?

Activmotion Range received FDA 510(k) clearance on 2018-02-27, under 510(k) number K173746.

Who is the listed applicant for Activmotion Range?

The FDA 510(k) record lists Newclip Technics as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Activmotion Range?

The FDA product code for Activmotion Range is HRS.

Other records listing Newclip Technics as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 26 devices →

Related Devices (Code: HRS)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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.