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

CODA AUTOMATED EIA ANALYZER

K Number: K972024 · Decision Jul 30, 1997
Classifications
1
FEI Numbers
5
Registration Numbers
5
Same Product Code
7
Applicant Total
319
Review Days
58

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Basic Information

Device Name
CODA AUTOMATED EIA ANALYZER
K Number
K972024
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.2500
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Bio-Rad
Date Received
June 2, 1997
Decision Date
July 30, 1997
Product Code
JJI
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
JJI Analyzer, Enzyme, For Clinical Use

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K100589 MRSA SELECT - SKIN AND SOFT TISSUE WOUND SPECIMENS
K081362 PLATELIA LYME IGM
K081212 MRSASELECT - EXTENDED INCUBATION
K080012 PLATELIA LYME IGG ASSAY
K070361 MRSASELECT
K060641 PLATELIA ASPERGILLUS EIA, MODEL 62793
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