FDA 510(k) FDA class 1 Substantially Equivalent 🇬🇧 United Kingdom

Randox RX Daytona Plus Magnesium (MG)

K Number: K162200 · Decision Apr 28, 2017
Classifications
1
FEI Numbers
44
Registration Numbers
44
Same Product Code
89
Applicant Total
116
Review Days
266

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Basic Information

Device Name
Randox RX Daytona Plus Magnesium (MG)
K Number
K162200
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1495
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Randox Laboratories, Ltd.
Date Received
August 5, 2016
Decision Date
April 28, 2017
Product Code
JGJ
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
JGJ Photometric Method, Magnesium

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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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