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QuikRead go CRP, QuikRead go CRP Verification Set, QuikRead go CRP Control Set, and QuikRead go Instrument

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K142993
510(k) Type
Traditional
Applicant
ORION DIAGNOSTICA OY
Country
Finland
FDA Decision
Substantially Equivalent
Decision Date
3/10/2016
Days to Decision
511 days
Submission Type
Statement

QuikRead go CRP, QuikRead go CRP Verification Set, QuikRead go CRP Control Set, and QuikRead go Instrument

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K142993
510(k) Type
Traditional
Applicant
ORION DIAGNOSTICA OY
Country
Finland
FDA Decision
Substantially Equivalent
Decision Date
3/10/2016
Days to Decision
511 days
Submission Type
Statement