i-Cut
K-번호: K243821 · 2025-04-25
광고
결정일2025-04-25
제품 코드HET
자문 위원회OB
결정Substantially Equivalent
기기 요약
i-Cut is the device name listed in this FDA 510(k) record. The listed applicant is A.M.I. Agency For Medical Innovations GmbH. It received FDA 510(k) clearance on 2025-04-25 under 510(k) number K243821. The device is classified under product code HET. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.
자주 묻는 질문
What is the i-Cut?
i-Cut is a medical device that received FDA 510(k) clearance on 2025-04-25. The listed applicant is A.M.I. Agency For Medical Innovations GmbH. The 510(k) number is K243821.
When did i-Cut receive FDA 510(k) clearance?
i-Cut received FDA 510(k) clearance on 2025-04-25, under 510(k) number K243821.
Who is the listed applicant for i-Cut?
The FDA 510(k) record lists A.M.I. Agency For Medical Innovations GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for i-Cut?
The FDA product code for i-Cut is HET.
관련 기기 (코드: HET)
관련 기록은 이름, 제품 코드 또는 기타 메타데이터를 사용하여 자동으로 매칭됩니다. 매칭은 검증된 임상, 과학, 기업 또는 규제 상의 관계를 입증하지 않으며, 연결된 공식 출처를 검토하시기 바랍니다.
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공식 출처
FDA 데이터베이스에서 보기 →FDA Open API에서 수집된 데이터입니다. 가장 정확하고 공인된 정보는 항상 공식 레코드를 참조하시기 바랍니다.
광고