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AURAFLEX FERRITIN 200 TEST PACK 80500, AURAFLEX FERRITIN CALIBRATOR PACK 80501

Page Type
Cleared 510(K)
510(k) Number
K974505
510(k) Type
Traditional
Applicant
ALFA BIOTECH (UK) LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
2/17/1998
Days to Decision
78 days
Submission Type
Summary

AURAFLEX FERRITIN 200 TEST PACK 80500, AURAFLEX FERRITIN CALIBRATOR PACK 80501

Page Type
Cleared 510(K)
510(k) Number
K974505
510(k) Type
Traditional
Applicant
ALFA BIOTECH (UK) LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
2/17/1998
Days to Decision
78 days
Submission Type
Summary