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RANDOX THERAPEUTIC DRUG CALIBRATOR

Page Type
Cleared 510(K)
510(k) Number
K012318
510(k) Type
Traditional
Applicant
RANDOX LABORATORIES, LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
9/12/2001
Days to Decision
51 days
Submission Type
Statement

RANDOX THERAPEUTIC DRUG CALIBRATOR

Page Type
Cleared 510(K)
510(k) Number
K012318
510(k) Type
Traditional
Applicant
RANDOX LABORATORIES, LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
9/12/2001
Days to Decision
51 days
Submission Type
Statement