Monitor de glucosa continuo, implantable, uso adyuvante
Número de PMA: P160048 · 2026-03-19
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Preguntas frecuentes
What is the Continuous glucose monitor, implanted, adjunctive use?
Continuous glucose monitor, implanted, adjunctive use is a medical device that received FDA 510(k) clearance on 2026-03-19. The listed applicant is Senseonics, Incorporated.
When did Continuous glucose monitor, implanted, adjunctive use receive FDA 510(k) clearance?
The clearance date for Continuous glucose monitor, implanted, adjunctive use can be found in the official FDA records.
Who is the listed applicant for Continuous glucose monitor, implanted, adjunctive use?
The FDA 510(k) record lists Senseonics, Incorporated as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Continuous glucose monitor, implanted, adjunctive use?
The FDA product code for Continuous glucose monitor, implanted, adjunctive use is QCD.
Ensayos clínicos relacionados
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Fuente oficial
Ver en la base de datos de la FDA →Datos procedentes de la API abierta de la FDA. Para obtener la información más actualizada y autoritativa, consulte siempre el registro oficial.
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