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FDA 510(k) Applications Submitted by JERALD STEINER
FDA 510(k) Number
Submission Date
Device Name
Applicant
K023362
10/07/2002
FISHER DIAGNOSTICS THROMBOSCREEN 1000; PACIFIC HEMOSTASIS FIBRINOGEN REAGENT PLUS KAOLIN
FISHER DIAGNOSTICS
K013397
10/15/2001
PACIFIC HEMOSTASIS REFERENCE EMULSION
FISHER DIAGNOSTICS
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