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FDA 510(k)

APEX NRG

K-Number: K032743 · 2004-03-15

Decision Date2004-03-15
Product CodeLQY
DecisionSubstantially Equivalent

Device Summary

APEX NRG is the device name listed in this FDA 510(k) record. The listed applicant is Medicnrg , Ltd.. It received FDA 510(k) clearance on 2004-03-15 under 510(k) number K032743. The device is classified under product code LQY. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the APEX NRG?

APEX NRG is a medical device that received FDA 510(k) clearance on 2004-03-15. The listed applicant is Medicnrg , Ltd.. The 510(k) number is K032743.

When did APEX NRG receive FDA 510(k) clearance?

APEX NRG received FDA 510(k) clearance on 2004-03-15, under 510(k) number K032743.

Who is the listed applicant for APEX NRG?

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 APEX NRG?

The FDA product code for APEX NRG is LQY.

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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