FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇦 Canada

DC-UIBC-CO2-CAL, MODEL SE-153

K Number: K013178 · Decision Dec 18, 2001
Classifications
1
FEI Numbers
101
Registration Numbers
101
Same Product Code
301
Applicant Total
66
Review Days
85

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Basic Information

Device Name
DC-UIBC-CO2-CAL, MODEL SE-153
K Number
K013178
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1150
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Diagnostic Chemicals , Ltd.
Date Received
September 24, 2001
Decision Date
December 18, 2001
Product Code
JIX
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
JIX Calibrator, Multi-Analyte Mixture

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K060139 CRP-ADVANCE ASSAY, MODELS 250-20, 250-25
K060140 CRP-ADVANCE MULTI CALIBRATOR SET, MODEL SE-250
K051757 CALCIUM ADVANCE ASSAY, MODEL 145-20, 145-25, 145-20-91
K051191 DCL MICROALBUMIN ASSAY, MODEL 252-20
K042330 ACETAMINOPHEN-SL ASSAY
K042329 SALICYLATE-SL ASSAY
K042362 MODIFICATION TO CARBON DIOXIDE-L3K ASSAY, CAT. NOS. 299-30, 299-17, 299-50, 299-80 AND 299-12
K041928 HDL-ADVANCE ASSAY, CAT. NO. 278-20, 278-50A, 278-50B
Search all 66 clearances from Diagnostic Chemicals , Ltd. →