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

BLOOD DILUTION VIAL

K Number: K844042 · Decision Oct 23, 1984
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
129
Applicant Total
28
Review Days
6

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Basic Information

Device Name
BLOOD DILUTION VIAL
K Number
K844042
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.5200
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
American Scientific Products
Date Received
October 17, 1984
Decision Date
October 23, 1984
Product Code
GKL
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
GKL Counter, Cell, Automated (Particle Counter)

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Other Clearances by American Scientific Products

K Number Device Name
K864824 INFECTIOUS TISSUE KIT
K831634 GLUCOSE REAGENT B6360-11
K831625 UREA NITROGEN-BUN-REAGENTS B6360-12
K831626 UREA NITROGEN-BUN-REAGENTS B6370-11A
K831628 CREATININE REAGENTS B6370-13
K831624 GLUCOSE REAGENT KITS-B6370-10A
K831627 CREATININE REAGENTS B6360-10
K831569 REAGENT CUPS
K831571 ROTOR
K822799 STREPTACOCCUS CO-AGGLUTINATION KIT
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