FDA 510(k)

VagiVital Aktivgel

N.º K: K200098 · 2020-11-10

Fecha de decisión2020-11-10

Código de productoNUC

Comité asesorOB

DecisiónSubstantially Equivalent

Resumen del dispositivo

VagiVital Aktivgel is the device name listed in this FDA 510(k) record. The listed applicant is Peptonic Medical AB. It received FDA 510(k) clearance on 2020-11-10 under 510(k) number K200098. The device is classified under product code NUC. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the VagiVital Aktivgel?

VagiVital Aktivgel is a medical device that received FDA 510(k) clearance on 2020-11-10. The listed applicant is Peptonic Medical AB. The 510(k) number is K200098.

When did VagiVital Aktivgel receive FDA 510(k) clearance?

VagiVital Aktivgel received FDA 510(k) clearance on 2020-11-10, under 510(k) number K200098.

Who is the listed applicant for VagiVital Aktivgel?

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

What is the FDA product code for VagiVital Aktivgel?

The FDA product code for VagiVital Aktivgel is NUC.

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