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FDA 510(k)

APEXNRG-BLUE ELECTRONIC APEX LOCATOR

K-Number: K071133 · 2007-09-21

Decision Date2007-09-21
Product CodeLQY
DecisionSubstantially Equivalent

Device Summary

APEXNRG-BLUE ELECTRONIC APEX LOCATOR is the device name listed in this FDA 510(k) record. The listed applicant is Medicnrg , Ltd.. It received FDA 510(k) clearance on 2007-09-21 under 510(k) number K071133. The device is classified under product code LQY. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the APEXNRG-BLUE ELECTRONIC APEX LOCATOR?

APEXNRG-BLUE ELECTRONIC APEX LOCATOR is a medical device that received FDA 510(k) clearance on 2007-09-21. The listed applicant is Medicnrg , Ltd.. The 510(k) number is K071133.

When did APEXNRG-BLUE ELECTRONIC APEX LOCATOR receive FDA 510(k) clearance?

APEXNRG-BLUE ELECTRONIC APEX LOCATOR received FDA 510(k) clearance on 2007-09-21, under 510(k) number K071133.

Who is the listed applicant for APEXNRG-BLUE ELECTRONIC APEX LOCATOR?

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-BLUE ELECTRONIC APEX LOCATOR?

The FDA product code for APEXNRG-BLUE ELECTRONIC APEX LOCATOR 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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