FDA 510(k)

ProVate Vaginal Support

N.º K: K190277 · 2019-07-08

Fecha de decisión2019-07-08

Código de productoHHW

Comité asesorOB

DecisiónSubstantially Equivalent

Resumen del dispositivo

ProVate Vaginal Support is the device name listed in this FDA 510(k) record. The listed applicant is Contipi Medical , Ltd.. It received FDA 510(k) clearance on 2019-07-08 under 510(k) number K190277. The device is classified under product code HHW. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the ProVate Vaginal Support?

ProVate Vaginal Support is a medical device that received FDA 510(k) clearance on 2019-07-08. The listed applicant is Contipi Medical , Ltd.. The 510(k) number is K190277.

When did ProVate Vaginal Support receive FDA 510(k) clearance?

ProVate Vaginal Support received FDA 510(k) clearance on 2019-07-08, under 510(k) number K190277.

Who is the listed applicant for ProVate Vaginal Support?

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

What is the FDA product code for ProVate Vaginal Support?

The FDA product code for ProVate Vaginal Support is HHW.

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Dispositivos relacionados (Código: HHW)

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Fuente oficial

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