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LIQUIDCHEK CARDIAC MARKERS PLUS CONTROL LT; LEVEL 1C, LEVEL 2, LEVEL 3, TRILEVEL MINIPAK

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K123663
510(k) Type
Traditional
Applicant
Bio-Rad Laboratories
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/27/2012
Days to Decision
29 days
Submission Type
Summary

LIQUIDCHEK CARDIAC MARKERS PLUS CONTROL LT; LEVEL 1C, LEVEL 2, LEVEL 3, TRILEVEL MINIPAK

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K123663
510(k) Type
Traditional
Applicant
Bio-Rad Laboratories
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/27/2012
Days to Decision
29 days
Submission Type
Summary