FDA 510(k)

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K-번호: K222164 · 2022-12-23

결정일2022-12-23

제품 코드LZU

결정대체적으로 동일

기기 요약

Visant Medical Canalicular Plug is the device name listed in this FDA 510(k) record. The listed applicant is Visant Medical, Inc.. It received FDA 510(k) clearance on 2022-12-23 under 510(k) number K222164. The device is classified under product code LZU. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the Visant Medical Canalicular Plug?

Visant Medical Canalicular Plug is a medical device that received FDA 510(k) clearance on 2022-12-23. The listed applicant is Visant Medical, Inc.. The 510(k) number is K222164.

When did Visant Medical Canalicular Plug receive FDA 510(k) clearance?

Visant Medical Canalicular Plug received FDA 510(k) clearance on 2022-12-23, under 510(k) number K222164.

Who is the listed applicant for Visant Medical Canalicular Plug?

The FDA 510(k) record lists Visant Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Visant Medical Canalicular Plug?

The FDA product code for Visant Medical Canalicular Plug is LZU.

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FDA Open API에서 수집된 데이터입니다. 가장 정확하고 공인된 정보는 항상 공식 레코드를 참조하시기 바랍니다.

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기기 요약

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관련 임상시험

관련 기기 (코드: LZU)

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