BE PLUS / AURA-LTM64 AMPLIFIER
K-Number: K053606 · 2006-01-24
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Device Summary
Frequently Asked Questions
What is the BE PLUS / AURA-LTM64 AMPLIFIER?
BE PLUS / AURA-LTM64 AMPLIFIER is a medical device that received FDA 510(k) clearance on 2006-01-24. The listed applicant is Eb Neuro S.P.A.. The 510(k) number is K053606.
When did BE PLUS / AURA-LTM64 AMPLIFIER receive FDA 510(k) clearance?
BE PLUS / AURA-LTM64 AMPLIFIER received FDA 510(k) clearance on 2006-01-24, under 510(k) number K053606.
Who is the listed applicant for BE PLUS / AURA-LTM64 AMPLIFIER?
The FDA 510(k) record lists Eb Neuro S.P.A. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BE PLUS / AURA-LTM64 AMPLIFIER?
The FDA product code for BE PLUS / AURA-LTM64 AMPLIFIER is GWL.
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 Eb Neuro S.P.A. 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: GWL)
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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