FDA 510(k) FDA class 1 Substantially Equivalent 🇩🇰 Denmark

AQT90 FLEX ANALYZER, AQT90 FLEX MYOGLOBIN TEST KIT, AQT90 FLEX LQC MULTI-CHECK, LVLS 1-3, AQT90 FLEX MYO CAL CARTRIDGE..

K Number: K112161 · Decision Jan 20, 2012
Classifications
1
FEI Numbers
51
Registration Numbers
51
Same Product Code
37
Applicant Total
28
Review Days
177

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
AQT90 FLEX ANALYZER, AQT90 FLEX MYOGLOBIN TEST KIT, AQT90 FLEX LQC MULTI-CHECK, LVLS 1-3, AQT90 FLEX MYO CAL CARTRIDGE..
K Number
K112161
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.2560
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Radiometer Medical Aps
Date Received
July 27, 2011
Decision Date
January 20, 2012
Product Code
KHO
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
KHO Fluorometer, For Clinical Use

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KHO), ordered by most recent decision date.

View all

Other Clearances by Radiometer Medical Aps

K Number Device Name
K163462 AQT90 FLEX Myo Test Kit, AQT90 FLEX CKMB Test Kit, AQT90 FLEX
K170882 ABL90 FLEX, ABL90 FLEX PLUS
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
Search all 28 clearances from Radiometer Medical Aps →