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FDA 510(k)

APEXNRG XFR

K-Number: K063843 · 2007-01-03

Decision Date2007-01-03
Product CodeLQY
DecisionSubstantially Equivalent

Device Summary

APEXNRG XFR is the device name listed in this FDA 510(k) record. The listed applicant is Medicnrg , Ltd.. It received FDA 510(k) clearance on 2007-01-03 under 510(k) number K063843. The device is classified under product code LQY. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the APEXNRG XFR?

APEXNRG XFR is a medical device that received FDA 510(k) clearance on 2007-01-03. The listed applicant is Medicnrg , Ltd.. The 510(k) number is K063843.

When did APEXNRG XFR receive FDA 510(k) clearance?

APEXNRG XFR received FDA 510(k) clearance on 2007-01-03, under 510(k) number K063843.

Who is the listed applicant for APEXNRG XFR?

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

What is the FDA product code for APEXNRG XFR?

The FDA product code for APEXNRG XFR is LQY.

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.

Other records listing Medicnrg , Ltd. 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.

Related Devices (Code: LQY)

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.

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.

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