Kitazato IUI Catheter
K-Number: K162667 · 2017-05-11
ApplicantKitazato Corporation
Decision Date2017-05-11
Product CodeMQF
Advisory CommitteeOB
DecisionSubstantially Equivalent
Device Summary
Kitazato IUI Catheter is a medical device manufactured by Kitazato Corporation. It received FDA 510(k) clearance on 2017-05-11 under approval number K162667. The device is classified under product code MQF. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Kitazato IUI Catheter?
Kitazato IUI Catheter is a medical device that received FDA 510(k) clearance on 2017-05-11. It is manufactured by Kitazato Corporation. The 510(k) number is K162667.
When was Kitazato IUI Catheter approved by the FDA?
Kitazato IUI Catheter received FDA 510(k) clearance on 2017-05-11, under approval number K162667.
What company makes Kitazato IUI Catheter?
Kitazato IUI Catheter is manufactured by Kitazato Corporation.
What is the FDA product code for Kitazato IUI Catheter?
The FDA product code for Kitazato IUI Catheter is MQF.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.