FDA 510(k) FDA class 2 Substantially Equivalent 🇬🇧 United Kingdom

Randox Calcium (Ca)

K Number: K182042 · Decision Oct 23, 2018
Classifications
1
FEI Numbers
29
Registration Numbers
29
Same Product Code
46
Applicant Total
116
Review Days
85

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Basic Information

Device Name
Randox Calcium (Ca)
K Number
K182042
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1145
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Randox Laboratories, Ltd.
Date Received
July 30, 2018
Decision Date
October 23, 2018
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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K153435 Direct HDL Cholesterol (HDL)
K150654 Cholesterol
K131554 RX DAYTONA PLUS CHEMISTRY ANALYZER; RX DAYTONA PLUS ASPARTATE AMINOTRANSFERASE (AST) REAGENT
K123977 RANDOX LIQUID CK-MB, RANDOX CK-MB CALIBRATOR
K132156 RANDOX CSF CONTROLS LEVELS 2 AND 3
K132090 BENZODIAZEPINE CALIBRATOR SET, BENZODIAZEPINE CONTROL LEVEL 1, AND BENZODIAZEPINE CONTROL LEVEL 2
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