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

CAROLINA LIQUID CHEMISTRIES HDL CHOLESTEROL REAGENT

K Number: K132711 · Decision May 8, 2014
Classifications
1
FEI Numbers
48
Registration Numbers
48
Same Product Code
79
Applicant Total
19
Review Days
252

Basic Information

Device Name
CAROLINA LIQUID CHEMISTRIES HDL CHOLESTEROL REAGENT
K Number
K132711
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1475
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
CAROLINA LIQUID CHEMISTRIES CORP.
Date Received
August 29, 2013
Decision Date
May 8, 2014
Product Code
LBS
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
LBS Ldl & Vldl Precipitation, Cholesterol Via Esterase-Oxidase, Hdl

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Other Clearances by CAROLINA LIQUID CHEMISTRIES CORP.

K Number Device Name
K133519 CAROLINA LIQUID CHEMISTRIES CLC 6410 CHEMISTRY ANALYZER; CAROLINA LIQUID CHEMISTRIES GLUCOSE REAGENT, CAR
K972073 TOTAL BILIRUBIN REAGENT
K971907 CALCIUM REAGENT
K971324 TRIGLYCERIDES, TG, OR TRIG
K971908 CREA OR CREATININE
K971967 BUN
K971467 SYNCHRON CX SYSTEMS GLUCOSE REAGENT (GLU)
K971396 CK REAGENT
K971345 CHOL OR CHOLESTEROL
K971524 TOTAL PROTEIN OR TP
Search all 19 clearances from CAROLINA LIQUID CHEMISTRIES CORP. →