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DIAMEDIX IS-ANTI-CARDIOLIPIN SCREEN TEST SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K012053
510(k) Type
Traditional
Applicant
Diamedix Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/20/2001
Days to Decision
49 days
Submission Type
Summary

DIAMEDIX IS-ANTI-CARDIOLIPIN SCREEN TEST SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K012053
510(k) Type
Traditional
Applicant
Diamedix Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/20/2001
Days to Decision
49 days
Submission Type
Summary