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ORGENTEC ANTI-CARDIOLIPIN SCREEN ELISA ASSAY

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K962926
510(k) Type
Traditional
Applicant
American Laboratory Products Co., Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/10/1996
Days to Decision
73 days
Submission Type
Summary

ORGENTEC ANTI-CARDIOLIPIN SCREEN ELISA ASSAY

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K962926
510(k) Type
Traditional
Applicant
American Laboratory Products Co., Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/10/1996
Days to Decision
73 days
Submission Type
Summary