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FDA 510(k)

Quiver Laparoscópica Extendible

N.º K: K153472 · 2016-06-23

SolicitanteItl Corporation Pty, Ltd.
Fecha de decisión2016-06-23
Código de productoHAM
Comité asesorSU
DecisiónSubstantially Equivalent

Resumen del dispositivo

Quiver Laparoscopic Extendable is the device name listed in this FDA 510(k) record. The listed applicant is Itl Corporation Pty, Ltd.. It received FDA 510(k) clearance on 2016-06-23 under 510(k) number K153472. The device is classified under product code HAM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Quiver Laparoscopic Extendable?

Quiver Laparoscopic Extendable is a medical device that received FDA 510(k) clearance on 2016-06-23. The listed applicant is Itl Corporation Pty, Ltd.. The 510(k) number is K153472.

When did Quiver Laparoscopic Extendable receive FDA 510(k) clearance?

Quiver Laparoscopic Extendable received FDA 510(k) clearance on 2016-06-23, under 510(k) number K153472.

Who is the listed applicant for Quiver Laparoscopic Extendable?

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

What is the FDA product code for Quiver Laparoscopic Extendable?

The FDA product code for Quiver Laparoscopic Extendable is HAM.

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Fuente oficial

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