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C-REACTIVE PROTEIN IMMUNOTURBIDIMETRIC KIT & CRP CALIBRATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K953212
510(k) Type
Traditional
Applicant
RANDOX LABORATORIES, LTD.
Country
Ireland
FDA Decision
Substantially Equivalent
Decision Date
7/31/1995
Days to Decision
21 days
Submission Type
Statement

C-REACTIVE PROTEIN IMMUNOTURBIDIMETRIC KIT & CRP CALIBRATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K953212
510(k) Type
Traditional
Applicant
RANDOX LABORATORIES, LTD.
Country
Ireland
FDA Decision
Substantially Equivalent
Decision Date
7/31/1995
Days to Decision
21 days
Submission Type
Statement