APEX NRG
K-Number: K032743 · 2004-03-15
Advertisement
Device Summary
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
Advertisement