FDA 510(k)

Miret Grasper, Alligator, Miret Grasper, Maryland

N.º K: K160149 · 2016-08-30

Fecha de decisión2016-08-30

Código de productoOCW

Comité asesorGU

DecisiónSubstantially Equivalent

Resumen del dispositivo

Miret Grasper, Alligator, Miret Grasper, Maryland is the device name listed in this FDA 510(k) record. The listed applicant is Miret Surgical, Inc.. It received FDA 510(k) clearance on 2016-08-30 under 510(k) number K160149. The device is classified under product code OCW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Miret Grasper, Alligator, Miret Grasper, Maryland?

Miret Grasper, Alligator, Miret Grasper, Maryland is a medical device that received FDA 510(k) clearance on 2016-08-30. The listed applicant is Miret Surgical, Inc.. The 510(k) number is K160149.

When did Miret Grasper, Alligator, Miret Grasper, Maryland receive FDA 510(k) clearance?

Miret Grasper, Alligator, Miret Grasper, Maryland received FDA 510(k) clearance on 2016-08-30, under 510(k) number K160149.

Who is the listed applicant for Miret Grasper, Alligator, Miret Grasper, Maryland?

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

What is the FDA product code for Miret Grasper, Alligator, Miret Grasper, Maryland?

The FDA product code for Miret Grasper, Alligator, Miret Grasper, Maryland is OCW.

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Fuente oficial

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