FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

DEMAND MAGNESIUM

K Number: K851657 · Decision May 10, 1985
Classifications
1
FEI Numbers
44
Registration Numbers
44
Same Product Code
89
Applicant Total
19
Review Days
17

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Basic Information

Device Name
DEMAND MAGNESIUM
K Number
K851657
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1495
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Cooper Biomedical, Inc.
Date Received
April 23, 1985
Decision Date
May 10, 1985
Product Code
JGJ
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

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

Product Code Device Name
JGJ Photometric Method, Magnesium

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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. →