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

LEAP LE TEST KIT

K Number: K842484 · Decision Jul 11, 1984
Classifications
1
FEI Numbers
18
Registration Numbers
18
Same Product Code
49
Applicant Total
19
Review Days
16

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Basic Information

Device Name
LEAP LE TEST KIT
K Number
K842484
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5100
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
Cooper Biomedical, Inc.
Date Received
June 25, 1984
Decision Date
July 11, 1984
Product Code
LKJ
Advisory Committee
Immunology
Review Advisory Committee
IM
Third Party
N

Classifications

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

Product Code Device Name
LKJ Antinuclear Antibody, Antigen, Control

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Other Clearances by Cooper Biomedical, Inc.

K Number Device Name
K863868 IMMUNO-PLATE IV RADIAL IMMUNO TEST KIT/ALPHA-1 ANT
K864512 IMMUNO-PLATE IV RADIAL IMMUNO TEST KIT/HUMAN HAPTO
K863301 DEMAND TOTAL PROTEIN
K861926 WORTHINGTON HDL PRECIPITATING REAGENT SET
K854130 DEMAND ETHYL ALCOHOL
K853949 DEMAND ACID PHOSPHATASE REAGENT
K852262 ASSIST CLINICAL CHEMISTRY ANALYZER
K851285 RADIAL IMMUNODIFFUSION PLATES CSF IGG & CSF ALBUMI
K851284 RADIAL IMMUNO-DIFFUSION PLATES IGA, IGD, IGG & IGM
K851286 RADIAL IMMUNODIFFUSION PLATES C3 & C4
Search all 19 clearances from Cooper Biomedical, Inc. →