FDA 510(k)

SoundBite Console, SoundBite Active Wire 18

N.º K: K192211 · 2020-01-17

SolicitanteSoundbite Medical Solution, Inc.

Fecha de decisión2020-01-17

Código de productoPDU

Comité asesorCV

DecisiónSubstantially Equivalent

Resumen del dispositivo

SoundBite Console, SoundBite Active Wire 18 is the device name listed in this FDA 510(k) record. The listed applicant is Soundbite Medical Solution, Inc.. It received FDA 510(k) clearance on 2020-01-17 under 510(k) number K192211. The device is classified under product code PDU. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the SoundBite Console, SoundBite Active Wire 18?

SoundBite Console, SoundBite Active Wire 18 is a medical device that received FDA 510(k) clearance on 2020-01-17. The listed applicant is Soundbite Medical Solution, Inc.. The 510(k) number is K192211.

When did SoundBite Console, SoundBite Active Wire 18 receive FDA 510(k) clearance?

SoundBite Console, SoundBite Active Wire 18 received FDA 510(k) clearance on 2020-01-17, under 510(k) number K192211.

Who is the listed applicant for SoundBite Console, SoundBite Active Wire 18?

The FDA 510(k) record lists Soundbite Medical Solution, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SoundBite Console, SoundBite Active Wire 18?

The FDA product code for SoundBite Console, SoundBite Active Wire 18 is PDU.

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Fuente oficial

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