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LYPHOCHEK COAGULATION CONTROL LEVEL 1, LYPHOCHEK COAGULATION LEVEL 2, LYPHOCHEK COAGULATION LEVEL 3, MODELS 781,782,783

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K012722
510(k) Type
Traditional
Applicant
Bio-Rad
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/18/2001
Days to Decision
34 days
Submission Type
Summary

LYPHOCHEK COAGULATION CONTROL LEVEL 1, LYPHOCHEK COAGULATION LEVEL 2, LYPHOCHEK COAGULATION LEVEL 3, MODELS 781,782,783

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K012722
510(k) Type
Traditional
Applicant
Bio-Rad
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/18/2001
Days to Decision
34 days
Submission Type
Summary