FDA 510(k) FDA class 2 Substantially Equivalent 🇫🇷 France

CARDIAC MARKERS ON ABX PENTRA 400 CLINICAL CHEMISTRY ANALYZER

K Number: K062737 · Decision Jun 12, 2007
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
122
Applicant Total
19
Review Days
272

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Basic Information

Device Name
CARDIAC MARKERS ON ABX PENTRA 400 CLINICAL CHEMISTRY ANALYZER
K Number
K062737
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1215
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Horiba Abx
Date Received
September 13, 2006
Decision Date
June 12, 2007
Product Code
CGS
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
CGS Nad Reduction/Nadh Oxidation, Cpk Or Isoenzymes

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Other Clearances by Horiba Abx

K Number Device Name
K073309 ABX PENTRA HBA1C WB, CALIBRATOR, CONTROL AND HEMOLYSIS REAGENT
K081276 ABX PENTRA GLUCOSE HK CP, ABX PENTRA URIC ACID CP, ABX PENTRA URINE CONTROL L/H
K071779 ABX PENTRA URINE CAL
K072115 ABX PENTRA CREATININE 120 CP, TOTAL PROTEIN 100 CP, MULTICAL, N AND P CONTROLS, AND URINE CONTROL L/H
K070146 ABX PENTRA GLUCOSE HK CP, UREA CP, URIC ACID CP
K060434 ABX PENTRA ALBUMIN CP, ABX PENTRA MICRO-ALBUMIN CP, ABX PENTRA TOTAL PROTEIN CP, ABX PENTRA MULTICAL
K070249 ABX PENTRA 400, CALCIUM CP, CREATININE CP, PHOSPHORUS CP, AMYLASE CP, URINE CONTROL L/H
K062180 ABX PENTRA AMYLASE CP; MULTICAL; N CONTROL; P CONTROL; CLEAN-CHEM CP; CLEAN-CHEM 99 CP
K061138 ABX PENTRA 400 : CRP
K060854 ABX PENTRA 400: LIPOPROTEINS
Search all 19 clearances from Horiba Abx →