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

ELECTROLYTE BUFFER A443-325, ELECTROLYTE REFERENCE REAGENT A443-315, CO2 ACID REAGENT A443-330, CO2 ALKALINE BUFFER A44

K Number: K982501 · Decision Sep 1, 1998
Classifications
1
FEI Numbers
107
Registration Numbers
107
Same Product Code
301
Applicant Total
31
Review Days
43

Basic Information

Device Name
ELECTROLYTE BUFFER A443-325, ELECTROLYTE REFERENCE REAGENT A443-315, CO2 ACID REAGENT A443-330, CO2 ALKALINE BUFFER A44
K Number
K982501
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1150
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
ALKO DIAGNOSTIC CORP.
Date Received
July 20, 1998
Decision Date
September 1, 1998
Product Code
JIX
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
JIX Calibrator, Multi-Analyte Mixture

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