FDA 510(k)

DV. Target

K-Number: K202928 · 2021-04-02

Decision Date2021-04-02

Product CodeQKB

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

DV. Target is the device name listed in this FDA 510(k) record. The listed applicant is Deepvoxel, Inc.. It received FDA 510(k) clearance on 2021-04-02 under 510(k) number K202928. The device is classified under product code QKB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DV. Target?

DV. Target is a medical device that received FDA 510(k) clearance on 2021-04-02. The listed applicant is Deepvoxel, Inc.. The 510(k) number is K202928.

When did DV. Target receive FDA 510(k) clearance?

DV. Target received FDA 510(k) clearance on 2021-04-02, under 510(k) number K202928.

Who is the listed applicant for DV. Target?

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

What is the FDA product code for DV. Target?

The FDA product code for DV. Target is QKB.

Related Devices (Code: QKB)

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.