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BIOPLEX 2200 EBV IGG PANEL FOR 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
K062211
510(k) Type
Traditional
Applicant
Bio-Rad Laboratories, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/8/2006
Days to Decision
129 days
Submission Type
Summary

BIOPLEX 2200 EBV IGG PANEL FOR 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
K062211
510(k) Type
Traditional
Applicant
Bio-Rad Laboratories, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/8/2006
Days to Decision
129 days
Submission Type
Summary