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VARELISA RECOMBI CTD SCREEN, MODEL 13096

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K050967
510(k) Type
Traditional
Applicant
SWEDEN DIAGNOSTICS (GERMANY) GMBH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
6/28/2005
Days to Decision
71 days
Submission Type
Summary

VARELISA RECOMBI CTD SCREEN, MODEL 13096

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K050967
510(k) Type
Traditional
Applicant
SWEDEN DIAGNOSTICS (GERMANY) GMBH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
6/28/2005
Days to Decision
71 days
Submission Type
Summary