FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

CARESIDE TRGLYCERIDE

K Number: K020488 · Decision Apr 15, 2002
Classifications
1
FEI Numbers
39
Registration Numbers
39
Same Product Code
150
Applicant Total
22
Review Days
61

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Basic Information

Device Name
CARESIDE TRGLYCERIDE
K Number
K020488
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1705
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Careside, Inc.
Date Received
February 13, 2002
Decision Date
April 15, 2002
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (CDT), ordered by most recent decision date.

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Other Clearances by Careside, Inc.

K Number Device Name
K020484 CARESIDE LDH
K020486 CARESIDE GGT
K020487 CARESIDE ALT
K002792 CARESIDE CHOLINESTERASE
K001462 CARESIDE HEMOGLOBIN
K993771 CARESIDE DIRECT BILIRUBIN
K993634 CARESIDE ANALYZER
K992475 CARESIDE CO2, TOTAL
K991717 CARESIDE MG
K991371 CARESIDE AMMONIA
Search all 22 clearances from Careside, Inc. →