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FDA 510(k)

ViMove2

K-Number: K163150 · 2017-07-14

ApplicantDorsavi, Ltd.
Decision Date2017-07-14
Product CodeIKN
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ViMove2 is the device name listed in this FDA 510(k) record. The listed applicant is Dorsavi, Ltd.. It received FDA 510(k) clearance on 2017-07-14 under 510(k) number K163150. The device is classified under product code IKN. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ViMove2?

ViMove2 is a medical device that received FDA 510(k) clearance on 2017-07-14. The listed applicant is Dorsavi, Ltd.. The 510(k) number is K163150.

When did ViMove2 receive FDA 510(k) clearance?

ViMove2 received FDA 510(k) clearance on 2017-07-14, under 510(k) number K163150.

Who is the listed applicant for ViMove2?

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

What is the FDA product code for ViMove2?

The FDA product code for ViMove2 is IKN.

Related Devices (Code: IKN)

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.

K172743Natus VikingQuestNatus Neurology IncorporatedK162383Cadwell Sierra Summit, Cadwell Sierra AscentCadwell Industries, Inc.

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.

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