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

PARAMAX ALKALINE PHOSPHATASE REAGENT-

K Number: K831480 · Decision Jun 22, 1983
Classifications
1
FEI Numbers
37
Registration Numbers
37
Same Product Code
123
Applicant Total
149
Review Days
44

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Basic Information

Device Name
PARAMAX ALKALINE PHOSPHATASE REAGENT-
K Number
K831480
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1050
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
American Dade
Date Received
May 9, 1983
Decision Date
June 22, 1983
Product Code
CJE
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
CJE Nitrophenylphosphate, Alkaline Phosphatase Or Isoenzymes

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Other Clearances by American Dade

K Number Device Name
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K873171 STRATUS(R) CK-MB FLUOROMETRIC ENZYME IMMUNOASSAY
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
Search all 149 clearances from American Dade →