FDA 510(k)

ACL TOP 970 CL, HemosIL CL Anti-Cardiolipina IgM, HemosIL CL Anti-ß2 Glicoproteína-I IgM

Número K: K221359 · 2023-09-29

Data da decisão2023-09-29

Código do produtoJPA

Comité consultivoHE

DecisãoSubstantially Equivalent

Resumo do dispositivo

ACL TOP 970 CL, HemosIL CL Anti-Cardiolipin IgM, HemosIL CL Anti-ß2 Glycoprotein-I IgM is the device name listed in this FDA 510(k) record. The listed applicant is Instrumentation Laboratory CO. It received FDA 510(k) clearance on 2023-09-29 under 510(k) number K221359. The device is classified under product code JPA. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the ACL TOP 970 CL, HemosIL CL Anti-Cardiolipin IgM, HemosIL CL Anti-ß2 Glycoprotein-I IgM?

ACL TOP 970 CL, HemosIL CL Anti-Cardiolipin IgM, HemosIL CL Anti-ß2 Glycoprotein-I IgM is a medical device that received FDA 510(k) clearance on 2023-09-29. The listed applicant is Instrumentation Laboratory CO. The 510(k) number is K221359.

When did ACL TOP 970 CL, HemosIL CL Anti-Cardiolipin IgM, HemosIL CL Anti-ß2 Glycoprotein-I IgM receive FDA 510(k) clearance?

ACL TOP 970 CL, HemosIL CL Anti-Cardiolipin IgM, HemosIL CL Anti-ß2 Glycoprotein-I IgM received FDA 510(k) clearance on 2023-09-29, under 510(k) number K221359.

Who is the listed applicant for ACL TOP 970 CL, HemosIL CL Anti-Cardiolipin IgM, HemosIL CL Anti-ß2 Glycoprotein-I IgM?

The FDA 510(k) record lists Instrumentation Laboratory CO as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ACL TOP 970 CL, HemosIL CL Anti-Cardiolipin IgM, HemosIL CL Anti-ß2 Glycoprotein-I IgM?

The FDA product code for ACL TOP 970 CL, HemosIL CL Anti-Cardiolipin IgM, HemosIL CL Anti-ß2 Glycoprotein-I IgM is JPA.

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Fonte oficial

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