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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 the device name listed in this FDA 510(k) record. The listed applicant is Inovytech Medical Solutions , Ltd.. It received FDA 510(k) clearance on 2021-01-29 under 510(k) 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. The listed applicant is Inovytech Medical Solutions , Ltd.. The 510(k) number is K202970.

When did Ventway Sparrow receive FDA 510(k) clearance?

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

Who is the listed applicant for Ventway Sparrow?

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

What is the FDA product code for Ventway Sparrow?

The FDA product code for Ventway Sparrow is CBK.

Related Devices (Code: CBK)

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.

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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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