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)

VRNT

K-Number: K230814 · 2023-10-31

ApplicantCognifisense, Inc.
Decision Date2023-10-31
Product CodeQRA
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

VRNT is a medical device manufactured by Cognifisense, Inc.. It received FDA 510(k) clearance on 2023-10-31 under approval number K230814. The device is classified under product code QRA. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VRNT?

VRNT is a medical device that received FDA 510(k) clearance on 2023-10-31. It is manufactured by Cognifisense, Inc.. The 510(k) number is K230814.

When was VRNT approved by the FDA?

VRNT received FDA 510(k) clearance on 2023-10-31, under approval number K230814.

What company makes VRNT?

VRNT is manufactured by Cognifisense, Inc..

What is the FDA product code for VRNT?

The FDA product code for VRNT is QRA.

Other Devices by Cognifisense, Inc.

K254004VRNT

Related Devices (Code: QRA)

DEN210014EaseVRxAppliedvr, Inc. K230825Smileyscope System (Therapy Mode)Smileyscope Holding, Inc. K243417RelieVRxAppliedvr K251519RelieVRx (Pico G3)Appliedvr K254004VRNTCognifisense, 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.

↑