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

RF-II TEST KIT

K Number: K801961 · Decision Oct 10, 1980
Classifications
1
FEI Numbers
59
Registration Numbers
59
Same Product Code
143
Applicant Total
8
Review Days
52

Basic Information

Device Name
RF-II TEST KIT
K Number
K801961
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5775
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
IMMUNO-DIAGNOSTIC PRODUCTS, INC.
Date Received
August 19, 1980
Decision Date
October 10, 1980
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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