Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

DV. Target

K-Number: K202928 · 2021-04-02

ApplicantDeepvoxel, Inc.
Decision Date2021-04-02
Product CodeQKB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DV. Target is a medical device manufactured by Deepvoxel, Inc.. It received FDA 510(k) clearance on 2021-04-02 under approval 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. It is manufactured by Deepvoxel, Inc.. The 510(k) number is K202928.

When was DV. Target approved by the FDA?

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

What company makes DV. Target?

DV. Target is manufactured by Deepvoxel, Inc..

What is the FDA product code for DV. Target?

The FDA product code for DV. Target is QKB.

Related Devices (Code: QKB)

K181572Workflow BoxMirada Medical, Ltd. K193562AI-Rad Companion Organs RTSiemens Medical Solutions USA, Inc. K200323AutoContourRadformation, Inc. K193252Contour ProtegeAIMim Software, Inc. K191928AccuContourXiamen Manteia Technology , Ltd. K213628VBrainVysioneer, 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.

↑