FDA 510(k)

Baha 5 Super Power Sound Processor

Número K: K153245 · 2016-03-02

Data da decisão2016-03-02

Código do produtoLXB

Comité consultivoEN

DecisãoSubstantially Equivalent

Resumo do dispositivo

Baha 5 Super Power Sound Processor is the device name listed in this FDA 510(k) record. The listed applicant is Cochlear Americas. It received FDA 510(k) clearance on 2016-03-02 under 510(k) number K153245. The device is classified under product code LXB. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Baha 5 Super Power Sound Processor?

Baha 5 Super Power Sound Processor is a medical device that received FDA 510(k) clearance on 2016-03-02. The listed applicant is Cochlear Americas. The 510(k) number is K153245.

When did Baha 5 Super Power Sound Processor receive FDA 510(k) clearance?

Baha 5 Super Power Sound Processor received FDA 510(k) clearance on 2016-03-02, under 510(k) number K153245.

Who is the listed applicant for Baha 5 Super Power Sound Processor?

The FDA 510(k) record lists Cochlear Americas as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Baha 5 Super Power Sound Processor?

The FDA product code for Baha 5 Super Power Sound Processor is LXB.

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Outros registros que listam Cochlear Americas como candidato(a)

K260902Cochlear™ Osia® 3(I) Sound Processor;Cochlear™ Osia® 3 Sound Processor;Cochlear™ Osia® 3 Charger;Cochlear™ Osia® 3 Aqua+;Cochlear™ Osia® Fitting Software 3;Cochlear™ Osia® Smart App;Cochlear™ Osia® System K240155Cochlear Osia System K231604Instrument Case K220922Cochlear Osia 2 System, Cochlear Osia OSI200 Implant, Cochlear Osia 2 Sound Processor, Cochlear Osia Fitting Software 2, Cochlear MRI Kit K212136Cochlear Baha 6 System, Cochlear Baha Fitting Software 6, Cochlear Baha Baha Smart App K202048Cochlear Baha 6 Max Sound Processor, Cochlear Baha Fitting Software 6, Cochlear Baha Smart App

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