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

ETHANOL CALIBRATOR

K Number: K872181 · Decision Jul 21, 1987
Classifications
1
FEI Numbers
41
Registration Numbers
41
Same Product Code
122
Applicant Total
73
Review Days
43

Basic Information

Device Name
ETHANOL CALIBRATOR
K Number
K872181
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3200
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Applicant
AMERICAN MONITOR CORP.
Date Received
June 8, 1987
Decision Date
July 21, 1987
Product Code
DLJ
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
DLJ Calibrators, Drug Specific

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