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ZEUS ANTI-CARDIOLIPIN IGS ELISA TEST SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K981020
510(k) Type
Traditional
Applicant
Zeus Scientific, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/18/1998
Days to Decision
60 days
Submission Type
Statement

ZEUS ANTI-CARDIOLIPIN IGS ELISA TEST SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K981020
510(k) Type
Traditional
Applicant
Zeus Scientific, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/18/1998
Days to Decision
60 days
Submission Type
Statement