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BIOPLEX 2200 HSV-1 AND HSV-2 IGG ON THE BIOPLEX 2200 MULTI-ANALYTE DETECTION SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K090409
510(k) Type
Traditional
Applicant
Bio-Rad Laboratories
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/8/2009
Days to Decision
79 days
Submission Type
Summary

BIOPLEX 2200 HSV-1 AND HSV-2 IGG ON THE BIOPLEX 2200 MULTI-ANALYTE DETECTION SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K090409
510(k) Type
Traditional
Applicant
Bio-Rad Laboratories
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/8/2009
Days to Decision
79 days
Submission Type
Summary