FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇪 Ireland

RHEUMATOID FACTOR LATEX SLIDE TEST KIT

K Number: K961169 · Decision Jun 26, 1996
Classifications
1
FEI Numbers
57
Registration Numbers
57
Same Product Code
143
Applicant Total
116
Review Days
93

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Basic Information

Device Name
RHEUMATOID FACTOR LATEX SLIDE TEST KIT
K Number
K961169
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5775
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Randox Laboratories, Ltd.
Date Received
March 25, 1996
Decision Date
June 26, 1996
Product Code
DHR
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
DHR System, Test, Rheumatoid Factor

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