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FDA 510(k)

APEXNRG RIDER

K-Number: K101177 · 2010-10-08

Decision Date2010-10-08
Product CodeLQY
DecisionSubstantially Equivalent

Device Summary

APEXNRG RIDER is the device name listed in this FDA 510(k) record. The listed applicant is Medicnrg , Ltd.. It received FDA 510(k) clearance on 2010-10-08 under 510(k) number K101177. The device is classified under product code LQY. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the APEXNRG RIDER?

APEXNRG RIDER is a medical device that received FDA 510(k) clearance on 2010-10-08. The listed applicant is Medicnrg , Ltd.. The 510(k) number is K101177.

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

APEXNRG RIDER received FDA 510(k) clearance on 2010-10-08, under 510(k) number K101177.

Who is the listed applicant for APEXNRG RIDER?

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 RIDER?

The FDA product code for APEXNRG RIDER 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

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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