FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇰 Denmark

AQT90 FLEX CKMB TEST KIT, AQT90 FLEX LQC MULTI-CHECK, LEVELS 1-3, AQT90 FLEX CKMB CAL CARTRIDGE

K Number: K120326 · Decision Nov 21, 2012
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
47
Applicant Total
28
Review Days
293

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Basic Information

Device Name
AQT90 FLEX CKMB TEST KIT, AQT90 FLEX LQC MULTI-CHECK, LEVELS 1-3, AQT90 FLEX CKMB CAL CARTRIDGE
K Number
K120326
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1215
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Radiometer Medical Aps
Date Received
February 2, 2012
Decision Date
November 21, 2012
Product Code
JHX
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
JHX Fluorometric Method, Cpk Or Isoenzymes

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Other Clearances by Radiometer Medical Aps

K Number Device Name
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K160153 ABL90 FLEX PLUS
K142898 ABL800 FLEX with AQURE connectivity
K150226 Hematocrit and Metabolite QUALICHECK
K132691 ABL90 FLEX
K131988 ABL90 FLEX ANALYZER
K130144 ABL90 FLEX
K123748 ABL90 FLEX
K130415 HIGH METABOLITE QUALICHECK
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