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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 the device name listed in this FDA 510(k) record. The listed applicant is Cognifisense, Inc.. It received FDA 510(k) clearance on 2023-10-31 under 510(k) 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. The listed applicant is Cognifisense, Inc.. The 510(k) number is K230814.

When did VRNT receive FDA 510(k) clearance?

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

Who is the listed applicant for VRNT?

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

What is the FDA product code for VRNT?

The FDA product code for VRNT is QRA.

Related Clinical Trials

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.

NCT07033195Virtual Reality Treatment for Adults With Chronic Back Pain (VRNT)ACTIVE_NOT_RECRUITING

Other records listing Cognifisense, Inc. as applicant

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.

K254004VRNT

Related Devices (Code: QRA)

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.

K254004VRNTCognifisense, Inc.K251519RelieVRx (Pico G3)AppliedvrK243417RelieVRxAppliedvrK230825Smileyscope System (Therapy Mode)Smileyscope Holding, 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.

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