FDA 510(k)

Kitazato IUI Catheter

Número K: K162667 · 2017-05-11

Data da decisão2017-05-11

Código do produtoMQF

Comité consultivoOB

DecisãoSubstantially Equivalent

Resumo do dispositivo

Kitazato IUI Catheter is the device name listed in this FDA 510(k) record. The listed applicant is Kitazato Corporation. It received FDA 510(k) clearance on 2017-05-11 under 510(k) number K162667. The device is classified under product code MQF. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Kitazato IUI Catheter?

Kitazato IUI Catheter is a medical device that received FDA 510(k) clearance on 2017-05-11. The listed applicant is Kitazato Corporation. The 510(k) number is K162667.

When did Kitazato IUI Catheter receive FDA 510(k) clearance?

Kitazato IUI Catheter received FDA 510(k) clearance on 2017-05-11, under 510(k) number K162667.

Who is the listed applicant for Kitazato IUI Catheter?

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

What is the FDA product code for Kitazato IUI Catheter?

The FDA product code for Kitazato IUI Catheter is MQF.

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