FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

LD-L REAGENT

K Number: K971398 · Decision May 2, 1997
Classifications
1
FEI Numbers
43
Registration Numbers
43
Same Product Code
110
Applicant Total
20
Review Days
17

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Basic Information

Device Name
LD-L REAGENT
K Number
K971398
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1440
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Carolina Liquid Chemistries Corp.
Date Received
April 15, 1997
Decision Date
May 2, 1997
Product Code
CFJ
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
CFJ Nad Reduction/Nadh Oxidation, Lactate Dehydrogenase

Similar 510(k) Clearances

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Other Clearances by Carolina Liquid Chemistries Corp.

K Number Device Name
K213211 Carolina Liquid Chemistries Cocaine and Cocaine Metabolite Enzyme Immunoassay (COCM) Test System
K133519 CAROLINA LIQUID CHEMISTRIES CLC 6410 CHEMISTRY ANALYZER; CAROLINA LIQUID CHEMISTRIES GLUCOSE REAGENT, CAR
K132711 CAROLINA LIQUID CHEMISTRIES HDL CHOLESTEROL REAGENT
K972073 TOTAL BILIRUBIN REAGENT
K971907 CALCIUM REAGENT
K971324 TRIGLYCERIDES, TG, OR TRIG
K971967 BUN
K971908 CREA OR CREATININE
K971467 SYNCHRON CX SYSTEMS GLUCOSE REAGENT (GLU)
K971345 CHOL OR CHOLESTEROL
Search all 20 clearances from Carolina Liquid Chemistries Corp. →