FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

FISHER DIAGNOSTICS THROMBOSCREEN 1000; PACIFIC HEMOSTASIS FIBRINOGEN REAGENT PLUS KAOLIN

K Number: K023362 · Decision Dec 9, 2002
Classifications
1
FEI Numbers
17
Registration Numbers
17
Same Product Code
48
Applicant Total
16
Review Days
63

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Basic Information

Device Name
FISHER DIAGNOSTICS THROMBOSCREEN 1000; PACIFIC HEMOSTASIS FIBRINOGEN REAGENT PLUS KAOLIN
K Number
K023362
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.5400
Medical Specialty
Hematology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Fisher Diagnostics
Date Received
October 7, 2002
Decision Date
December 9, 2002
Product Code
GKP
Advisory Committee
Hematology
Review Advisory Committee
HE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GKP Instrument, Coagulation, Automated

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K052407 ARCHITECT ANTI-TPO IMMUNOASSAY, CALIBRATORS & CONTROLS
K052308 ARCHITECT ANTI-TG IMMUNOASSAY REAGENTS, CALIBRATORS, CONTROLS AND SYSTEM ASSAY CD-ROM
K042924 ARCHITECT STAT MYO IMMUNOASSAY
K041192 ARCHITECT STAT TROPONIN-I IMMUNOASSAY
K041596 ARCHITECT STAT CK-MB IMMUNOASSAY
K013397 PACIFIC HEMOSTASIS REFERENCE EMULSION
K010750 PACIFIC HEMOSTASIS INR CONTROL PLASMAS, MODEL CATALOG 100560
K850160 FISHER DIAGNOSTICS LATEST-CRP TEST KIT
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