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FDA 510(k)

BIAFINE Topical Cream

N.º K: K190342 · 2019-10-18

SolicitanteBausch Health Americas Incorporated
Fecha de decisión2019-10-18
Código de productoFRO
DecisiónSubstantially Equivalent

Resumen del dispositivo

BIAFINE Topical Cream is the device name listed in this FDA 510(k) record. The listed applicant is Bausch Health Americas Incorporated. It received FDA 510(k) clearance on 2019-10-18 under 510(k) number K190342. The device is classified under product code FRO. Product code FRO falls under the category of Anesthesiology, which includes devices for anesthetic delivery and patient monitoring. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the BIAFINE Topical Cream?

BIAFINE Topical Cream is a medical device that received FDA 510(k) clearance on 2019-10-18. The listed applicant is Bausch Health Americas Incorporated. The 510(k) number is K190342.

When did BIAFINE Topical Cream receive FDA 510(k) clearance?

BIAFINE Topical Cream received FDA 510(k) clearance on 2019-10-18, under 510(k) number K190342.

Who is the listed applicant for BIAFINE Topical Cream?

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

What is the FDA product code for BIAFINE Topical Cream?

The FDA product code for BIAFINE Topical Cream is FRO. This falls under the Anesthesiology category.

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Fuente oficial

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