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

DEMAND ETHYL ALCOHOL

K Number: K854130 · Decision Nov 5, 1985
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
32
Applicant Total
19
Review Days
27

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Basic Information

Device Name
DEMAND ETHYL ALCOHOL
K Number
K854130
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3040
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Applicant
Cooper Biomedical, Inc.
Date Received
October 9, 1985
Decision Date
November 5, 1985
Product Code
DIC
Advisory Committee
Clinical Toxicology
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
DIC Alcohol Dehydrogenase, Specific Reagent For Ethanol Enzyme Method

Similar 510(k) Clearances

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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
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
K851282 RADIAL IMMUNODIFFUSION PLATES ALPHA-2 MACROGLOBULI
Search all 19 clearances from Cooper Biomedical, Inc. →