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FDA 510(k)

NET Recovery Corp/NET Device

K-Number: K233166 · 2024-05-29

ApplicantNet Recovery
Decision Date2024-05-29
Product CodePZR
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

NET Recovery Corp/NET Device is a medical device manufactured by Net Recovery. It received FDA 510(k) clearance on 2024-05-29 under approval number K233166. The device is classified under product code PZR. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NET Recovery Corp/NET Device?

NET Recovery Corp/NET Device is a medical device that received FDA 510(k) clearance on 2024-05-29. It is manufactured by Net Recovery. The 510(k) number is K233166.

When was NET Recovery Corp/NET Device approved by the FDA?

NET Recovery Corp/NET Device received FDA 510(k) clearance on 2024-05-29, under approval number K233166.

What company makes NET Recovery Corp/NET Device?

NET Recovery Corp/NET Device is manufactured by Net Recovery.

What is the FDA product code for NET Recovery Corp/NET Device?

The FDA product code for NET Recovery Corp/NET Device is PZR.

Related Clinical Trials

Related Devices (Code: PZR)

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.