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BioPlex 2200 Syphilis Total & RPR, BioPlex 2200 Syphilis Total & RPR Calibrator Set, BioPlex 2200 Syphilis Total & RPR Control Set

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K170413
510(k) Type
Traditional
Applicant
Bio-Rad Laboratories
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/11/2017
Days to Decision
90 days
Submission Type
Summary

BioPlex 2200 Syphilis Total & RPR, BioPlex 2200 Syphilis Total & RPR Calibrator Set, BioPlex 2200 Syphilis Total & RPR Control Set

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K170413
510(k) Type
Traditional
Applicant
Bio-Rad Laboratories
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/11/2017
Days to Decision
90 days
Submission Type
Summary