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FDA 510(k)

RelieVRx

K-Number: K243417 · 2024-12-04

ApplicantAppliedvr
Decision Date2024-12-04
Product CodeQRA
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

RelieVRx is a medical device manufactured by Appliedvr. It received FDA 510(k) clearance on 2024-12-04 under approval number K243417. 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 RelieVRx?

RelieVRx is a medical device that received FDA 510(k) clearance on 2024-12-04. It is manufactured by Appliedvr. The 510(k) number is K243417.

When was RelieVRx approved by the FDA?

RelieVRx received FDA 510(k) clearance on 2024-12-04, under approval number K243417.

What company makes RelieVRx?

RelieVRx is manufactured by Appliedvr.

What is the FDA product code for RelieVRx?

The FDA product code for RelieVRx is QRA.

Other Devices by Appliedvr

K251519RelieVRx (Pico G3)

Related Devices (Code: QRA)

DEN210014EaseVRxAppliedvr, Inc. K230814VRNTCognifisense, Inc. K230825Smileyscope System (Therapy Mode)Smileyscope Holding, Inc. 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.

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