FDA 510(k)

MAUSER PG II Sharps Container

N.º K: K170513 · 2017-11-01

Fecha de decisión2017-11-01

Código de productoMMK

Comité asesorHO

DecisiónSubstantially Equivalent

Resumen del dispositivo

MAUSER PG II Sharps Container is the device name listed in this FDA 510(k) record. The listed applicant is Mauzer USA, LLC. It received FDA 510(k) clearance on 2017-11-01 under 510(k) number K170513. The device is classified under product code MMK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the MAUSER PG II Sharps Container?

MAUSER PG II Sharps Container is a medical device that received FDA 510(k) clearance on 2017-11-01. The listed applicant is Mauzer USA, LLC. The 510(k) number is K170513.

When did MAUSER PG II Sharps Container receive FDA 510(k) clearance?

MAUSER PG II Sharps Container received FDA 510(k) clearance on 2017-11-01, under 510(k) number K170513.

Who is the listed applicant for MAUSER PG II Sharps Container?

The FDA 510(k) record lists Mauzer USA, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MAUSER PG II Sharps Container?

The FDA product code for MAUSER PG II Sharps Container is MMK.

Ensayos clínicos relacionados

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Dispositivos relacionados (Código: MMK)

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