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

Triglycerides

K Number: K150819 · Decision Aug 6, 2015
Classifications
1
FEI Numbers
39
Registration Numbers
39
Same Product Code
150
Applicant Total
18
Review Days
132

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Basic Information

Device Name
Triglycerides
K Number
K150819
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1705
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Randox Laboratories Limited
Date Received
March 27, 2015
Decision Date
August 6, 2015
Product Code
CDT
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
CDT Lipase Hydrolysis/Glycerol Kinase Enzyme, Triglycerides

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K161691 Direct LDL Cholesterol (LDL)
K152343 Direct Bilirubin
K152344 Total Bilirubin
K140971 LIQUID ASSAYED CHEMISTRY CONTROL PREMIUM PLUS LEVEL 1,2 AND LEVEL 3.
K142181 RANDOX ALDOLASE CALIBRATION SERUM
K140522 RANDOX IMMUNOASSAY PREMIUM PLUS CONTROL LEVELS 1,2 AND LEVEL 3 AND IMMUNOASSAY PREMIUM PLUS TRI-LEVEL CONTROL
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