FDA 510(k)

NET Recovery Corp/NET Device

K-Number: K233166 · 2024-05-29

Decision Date2024-05-29

Product CodePZR

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

NET Recovery Corp/NET Device is the device name listed in this FDA 510(k) record. The listed applicant is Net Recovery. It received FDA 510(k) clearance on 2024-05-29 under 510(k) 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. The listed applicant is Net Recovery. The 510(k) number is K233166.

When did NET Recovery Corp/NET Device receive FDA 510(k) clearance?

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

Who is the listed applicant for NET Recovery Corp/NET Device?

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

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 Devices (Code: PZR)

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.

K251246Sparrow AscentSpark Biomedical, Inc.K230796Sparrow AscentSpark Biomedical, Inc.K221231Drug Relief v1Dyansys, Inc.K211971Drug Relief v1Dyansys, Inc.K201873Sparrow Therapy SystemSpark Biomedical, Inc.K173861Drug ReliefDyansys, Inc.

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.