ACL TOP 970 CL
K-번호: K233790 · 2023-12-29
광고
기기 요약
ACL TOP 970 CL is the device name listed in this FDA 510(k) record. The listed applicant is Instrumentation Laboratory. It received FDA 510(k) clearance on 2023-12-29 under 510(k) number K233790. The device is classified under product code JPA. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.
자주 묻는 질문
What is the ACL TOP 970 CL?
ACL TOP 970 CL is a medical device that received FDA 510(k) clearance on 2023-12-29. The listed applicant is Instrumentation Laboratory. The 510(k) number is K233790.
When did ACL TOP 970 CL receive FDA 510(k) clearance?
ACL TOP 970 CL received FDA 510(k) clearance on 2023-12-29, under 510(k) number K233790.
Who is the listed applicant for ACL TOP 970 CL?
The FDA 510(k) record lists Instrumentation Laboratory as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ACL TOP 970 CL?
The FDA product code for ACL TOP 970 CL is JPA.
관련 기기 (코드: JPA)
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