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

CHLORIDE/CARBON DIOXIDE RATE REAGENT

K Number: K811701 · Decision Jul 1, 1981
Classifications
1
FEI Numbers
2
Registration Numbers
2
Same Product Code
18
Applicant Total
9
Review Days
15

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Basic Information

Device Name
CHLORIDE/CARBON DIOXIDE RATE REAGENT
K Number
K811701
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1170
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Chem-Elec, Inc.
Date Received
June 16, 1981
Decision Date
July 1, 1981
Product Code
JFS
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
JFS Coulometric, Chloride

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Other Clearances by Chem-Elec, Inc.

K Number Device Name
K943503 CHEMCARD GLUCOSE TEST
K864159 SOLID PHASE DETER SERUM CHOLESTEROL FR WHOLE BLOOD
K811165 GLUCOSE OXIDASE RATE REAGENT
K811406 CREATININE RATE REAGENT KIT
K811381 ASTRA
K811319 CHLORIDE REAGENT KIT
K811193 BUN RATE REAGENT
K811310 SODIUM/POTASSIUM REAGENT KITS