Bencox Mirabo Cup System
K-Number: K172806 · 2017-10-17
ApplicantCorentec Co., Ltd.
Decision Date2017-10-17
Product CodeLPH
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Bencox Mirabo Cup System is a medical device manufactured by Corentec Co., Ltd.. It received FDA 510(k) clearance on 2017-10-17 under approval number K172806. The device is classified under product code LPH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Bencox Mirabo Cup System?
Bencox Mirabo Cup System is a medical device that received FDA 510(k) clearance on 2017-10-17. It is manufactured by Corentec Co., Ltd.. The 510(k) number is K172806.
When was Bencox Mirabo Cup System approved by the FDA?
Bencox Mirabo Cup System received FDA 510(k) clearance on 2017-10-17, under approval number K172806.
What company makes Bencox Mirabo Cup System?
Bencox Mirabo Cup System is manufactured by Corentec Co., Ltd..
What is the FDA product code for Bencox Mirabo Cup System?
The FDA product code for Bencox Mirabo Cup System is LPH.
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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.