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

CALCIUM ADVANCE ASSAY, MODEL 145-20, 145-25, 145-20-91

K Number: K051757 · Decision Nov 10, 2005
Classifications
1
FEI Numbers
29
Registration Numbers
29
Same Product Code
46
Applicant Total
66
Review Days
134

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Basic Information

Device Name
CALCIUM ADVANCE ASSAY, MODEL 145-20, 145-25, 145-20-91
K Number
K051757
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1145
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Diagnostic Chemicals , Ltd.
Date Received
June 29, 2005
Decision Date
November 10, 2005
Product Code
CJY
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
CJY Azo Dye, Calcium

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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
K041926 HDL/LDL-ADVANCE CALIBRATOR, CAT. NO. SE-278
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