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

ENA EIA KIT

K Number: K010147 · Decision Mar 1, 2001
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
179
Applicant Total
115
Review Days
43

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Basic Information

Device Name
ENA EIA KIT
K Number
K010147
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5100
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
The Binding Site, Ltd.
Date Received
January 17, 2001
Decision Date
March 1, 2001
Product Code
LLL
Advisory Committee
Immunology
Review Advisory Committee
IM
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LLL Extractable Antinuclear Antibody, Antigen And Control

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K083289 HUMAN BETA-2 MICROGLOBULIN KIT
K082129 HUMAN IGM LIQUID REAGENT KIT FOR USE ON THE SPAPLUS ANALYZER
K081827 HUMAN IGA LIQUID REAGENT KIT FOR USE ON SPAPLUS
K081674 BINDAZYME HUMAN ANTI-GLIADIN (MGP), IGG EIA KIT; BINDAZYME HUMAN ANTI-GLIADIN (MGP) IGA EIA KIT; (IGA OR IGG)
K080384 HUMAN CYSTATIN C KIT FOR USE ON MODULAR P ANALYSER
K072889 HUMAN IGG SUBCLASS LIQUID REAGENT KITS FOR USE ON THE SPAPLUS ANALYSER
K070900 FREELITE HUMAN KAPPA AND LAMBDA FREE DIAGNOSTIC TEST KITS FOR USE ON THE ROCHE COBAS INTEGRA 400/400 PLUS ANALYZER KIT
K062372 FREELITE HUMAN KAPPA AND LAMBDA FREE KITS FOR USE ON THE SPAPLUS ANALYZER
Search all 115 clearances from The Binding Site, Ltd. →