FDA 510(k)

Sporview VH202 BI

N.º K: K171287 · 2018-02-01

SolicitanteSpsmedical Supply Corp. A Division of Cantel Medical

Fecha de decisión2018-02-01

Código de productoFRC

Comité asesorHO

DecisiónSubstantially Equivalent

Resumen del dispositivo

Sporview VH202 BI is the device name listed in this FDA 510(k) record. The listed applicant is Spsmedical Supply Corp. A Division of Cantel Medical. It received FDA 510(k) clearance on 2018-02-01 under 510(k) number K171287. The device is classified under product code FRC. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Sporview VH202 BI?

Sporview VH202 BI is a medical device that received FDA 510(k) clearance on 2018-02-01. The listed applicant is Spsmedical Supply Corp. A Division of Cantel Medical. The 510(k) number is K171287.

When did Sporview VH202 BI receive FDA 510(k) clearance?

Sporview VH202 BI received FDA 510(k) clearance on 2018-02-01, under 510(k) number K171287.

Who is the listed applicant for Sporview VH202 BI?

The FDA 510(k) record lists Spsmedical Supply Corp. A Division of Cantel Medical as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Sporview VH202 BI?

The FDA product code for Sporview VH202 BI is FRC.

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Fuente oficial

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