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FDA 510(k)

Ventway Sparrow

K-Number: K202970 · 2021-01-29

ApplicantInovytech Medical Solutions , Ltd.
Decision Date2021-01-29
Product CodeCBK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

Ventway Sparrow is a medical device manufactured by Inovytech Medical Solutions , Ltd.. It received FDA 510(k) clearance on 2021-01-29 under approval number K202970. The device is classified under product code CBK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Ventway Sparrow?

Ventway Sparrow is a medical device that received FDA 510(k) clearance on 2021-01-29. It is manufactured by Inovytech Medical Solutions , Ltd.. The 510(k) number is K202970.

When was Ventway Sparrow approved by the FDA?

Ventway Sparrow received FDA 510(k) clearance on 2021-01-29, under approval number K202970.

What company makes Ventway Sparrow?

Ventway Sparrow is manufactured by Inovytech Medical Solutions , Ltd..

What is the FDA product code for Ventway Sparrow?

The FDA product code for Ventway Sparrow is CBK.

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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.

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