FDA 510(k)

MAUSER PG II Sharps Container

Numéro K : K170513 · 2017-11-01

Date de décision2017-11-01

Code produitMMK

Comité consultatifHO

DécisionSubstantially Equivalent

Résumé du dispositif

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.

Questions fréquentes

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.

Essais cliniques associés

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Dispositifs connexes (Code : MMK)

Source officielle

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