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

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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