BENCOX Mirabo Z Cup Cortinium
K-Number: K223223 · 2023-02-27
ApplicantCorentec Co., Ltd.
Decision Date2023-02-27
Product CodeLPH
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
BENCOX Mirabo Z Cup Cortinium is a medical device manufactured by Corentec Co., Ltd.. It received FDA 510(k) clearance on 2023-02-27 under approval number K223223. 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 Z Cup Cortinium?
BENCOX Mirabo Z Cup Cortinium is a medical device that received FDA 510(k) clearance on 2023-02-27. It is manufactured by Corentec Co., Ltd.. The 510(k) number is K223223.
When was BENCOX Mirabo Z Cup Cortinium approved by the FDA?
BENCOX Mirabo Z Cup Cortinium received FDA 510(k) clearance on 2023-02-27, under approval number K223223.
What company makes BENCOX Mirabo Z Cup Cortinium?
BENCOX Mirabo Z Cup Cortinium is manufactured by Corentec Co., Ltd..
What is the FDA product code for BENCOX Mirabo Z Cup Cortinium?
The FDA product code for BENCOX Mirabo Z Cup Cortinium 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.