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

CARBON DIOXIDE CALIBRATOR II

K Number: K840775 · Decision Apr 4, 1984
Classifications
1
FEI Numbers
126
Registration Numbers
126
Same Product Code
244
Applicant Total
149
Review Days
56

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Basic Information

Device Name
CARBON DIOXIDE CALIBRATOR II
K Number
K840775
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1150
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
American Dade
Date Received
February 8, 1984
Decision Date
April 4, 1984
Product Code
JIT
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
JIT Calibrator, Secondary

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K873052 STRATUS(R) HLH FLUOROMETRIC ENZYME IMMUNOASSAY
K872789 PARAMAX URINE/CSF CALIBRATOR
K872195 DATA-FI DIMERTEST LATEX ASSAY
K872196 AQUEOUS BLOOD GAS/ELECTROLYTE CONTR LEV I,II & III
K871972 STRATUS IGE FLUOROMETRIC ENZYME IMMUNOASSAY
K871977 DADE MONI-TROL CHEMISTRY CONTROL/CALIBRATOR
K872050 PARAMAX CHOLESTEROL REAGENT
K872360 DATA-FI FIBRIN(OGEN) DEGRADATION PROD.(FDP)DET SET
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