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

KINETIC 610 ETHANOL

K Number: K872180 · Decision Jul 7, 1987
Classifications
1
FEI Numbers
6
Registration Numbers
6
Same Product Code
12
Applicant Total
73
Review Days
29

Basic Information

Device Name
KINETIC 610 ETHANOL
K Number
K872180
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3040
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Applicant
AMERICAN MONITOR CORP.
Date Received
June 8, 1987
Decision Date
July 7, 1987
Product Code
DML
Advisory Committee
Clinical Toxicology
Review Advisory Committee
TX
Third Party
N

Classifications

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

Product Code Device Name
DML Nad-Nadh, Specific Reagent For Alcohol Enzyme Method

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K893137 EXCEL (TM) CHEMISTRY ANALYZER
K892331 ENZYMATIC UREA NITROGEN REAGENT SET
K893479 CHOLESTEROL REAGENT SET
K892002 NEOCHROME(R) III GLUCOSE
K890312 GAMMA-GLUTAMYLTRANSFERASE
K890034 PHOTOMETRIC METHOD, IRON (NON-HEME) (75JIY)
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