결정일2018-06-22
제품 코드LEJ
자문 위원회SU
결정Substantially Equivalent
기기 요약
UV Lamps for Sunlamp Products is the device name listed in this FDA 510(k) record. The listed applicant is Feilo Sylvania Germany GmbH. It received FDA 510(k) clearance on 2018-06-22 under 510(k) number K180581. The device is classified under product code LEJ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
자주 묻는 질문
What is the UV Lamps for Sunlamp Products?
UV Lamps for Sunlamp Products is a medical device that received FDA 510(k) clearance on 2018-06-22. The listed applicant is Feilo Sylvania Germany GmbH. The 510(k) number is K180581.
When did UV Lamps for Sunlamp Products receive FDA 510(k) clearance?
UV Lamps for Sunlamp Products received FDA 510(k) clearance on 2018-06-22, under 510(k) number K180581.
Who is the listed applicant for UV Lamps for Sunlamp Products?
The FDA 510(k) record lists Feilo Sylvania Germany GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for UV Lamps for Sunlamp Products?
The FDA product code for UV Lamps for Sunlamp Products is LEJ.
관련 임상시험
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.
관련 기기 (코드: LEJ)
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.