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ORION DIAGNOSTICA QUIKREAD CRP KIT AND QUIKREAD CRP CONTROL

Page Type
Cleared 510(K)
510(k) Number
K031607
510(k) Type
Traditional
Applicant
ORION DIAGNOSTICA, DIV. ORION CORP.
Country
Finland
FDA Decision
Substantially Equivalent
Decision Date
10/10/2003
Days to Decision
141 days
Submission Type
Statement

ORION DIAGNOSTICA QUIKREAD CRP KIT AND QUIKREAD CRP CONTROL

Page Type
Cleared 510(K)
510(k) Number
K031607
510(k) Type
Traditional
Applicant
ORION DIAGNOSTICA, DIV. ORION CORP.
Country
Finland
FDA Decision
Substantially Equivalent
Decision Date
10/10/2003
Days to Decision
141 days
Submission Type
Statement