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ACL TOP 970 CL, HemosIL CL Anti-Cardiolipin IgM, HemosIL CL Anti-ß2 Glycoprotein-I IgM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221359
510(k) Type
Traditional
Applicant
Instrumentation Laboratory CO
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/29/2023
Days to Decision
506 days
Submission Type
Summary

ACL TOP 970 CL, HemosIL CL Anti-Cardiolipin IgM, HemosIL CL Anti-ß2 Glycoprotein-I IgM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221359
510(k) Type
Traditional
Applicant
Instrumentation Laboratory CO
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/29/2023
Days to Decision
506 days
Submission Type
Summary