BE PLUS LTM AMPLIFIER GWI AMPLIFIER
K-Number: K121996 · 2012-08-03
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Device Summary
Frequently Asked Questions
What is the BE PLUS LTM AMPLIFIER GWI AMPLIFIER?
BE PLUS LTM AMPLIFIER GWI AMPLIFIER is a medical device that received FDA 510(k) clearance on 2012-08-03. The listed applicant is Eb Neuro S.P.A.. The 510(k) number is K121996.
When did BE PLUS LTM AMPLIFIER GWI AMPLIFIER receive FDA 510(k) clearance?
BE PLUS LTM AMPLIFIER GWI AMPLIFIER received FDA 510(k) clearance on 2012-08-03, under 510(k) number K121996.
Who is the listed applicant for BE PLUS LTM AMPLIFIER GWI 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 LTM AMPLIFIER GWI AMPLIFIER?
The FDA product code for BE PLUS LTM AMPLIFIER GWI 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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