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FDA 510(k)

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 the device name listed in this FDA 510(k) record. The listed applicant is Corentec Co., Ltd.. It received FDA 510(k) clearance on 2023-02-27 under 510(k) 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. The listed applicant is Corentec Co., Ltd.. The 510(k) number is K223223.

When did BENCOX Mirabo Z Cup Cortinium receive FDA 510(k) clearance?

BENCOX Mirabo Z Cup Cortinium received FDA 510(k) clearance on 2023-02-27, under 510(k) number K223223.

Who is the listed applicant for BENCOX Mirabo Z Cup Cortinium?

The FDA 510(k) record lists Corentec Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BENCOX Mirabo Z Cup Cortinium?

The FDA product code for BENCOX Mirabo Z Cup Cortinium is LPH.

Other records listing Corentec Co., Ltd. as applicant

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Related Devices (Code: 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.

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