FDA 510(k)

Mochida Nerve Cuff

K-번호: K233322 · 2024-06-21

결정일2024-06-21

제품 코드JXI

자문 위원회NE

결정Substantially Equivalent

기기 요약

Mochida Nerve Cuff is the device name listed in this FDA 510(k) record. The listed applicant is Mochida Pharmaceutical Co., Ltd.. It received FDA 510(k) clearance on 2024-06-21 under 510(k) number K233322. The device is classified under product code JXI. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the Mochida Nerve Cuff?

Mochida Nerve Cuff is a medical device that received FDA 510(k) clearance on 2024-06-21. The listed applicant is Mochida Pharmaceutical Co., Ltd.. The 510(k) number is K233322.

When did Mochida Nerve Cuff receive FDA 510(k) clearance?

Mochida Nerve Cuff received FDA 510(k) clearance on 2024-06-21, under 510(k) number K233322.

Who is the listed applicant for Mochida Nerve Cuff?

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

What is the FDA product code for Mochida Nerve Cuff?

The FDA product code for Mochida Nerve Cuff is JXI.

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Mochida Nerve Cuff

기기 요약

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관련 임상시험

관련 기기 (코드: JXI)

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