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

TEST, RHEUMATOID FACTOR

K Number: K955086 · Decision Dec 20, 1995
Classifications
1
FEI Numbers
57
Registration Numbers
57
Same Product Code
143
Applicant Total
19
Review Days
43

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Basic Information

Device Name
TEST, RHEUMATOID FACTOR
K Number
K955086
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5775
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Polymedco, Inc.
Date Received
November 7, 1995
Decision Date
December 20, 1995
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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K090703 POLY-CHEM 90 GLUCOSE
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K053553 NYCOCARD U-ALBUMIN AND U-ALBUMIN CONTROL
K041408 POLYMEDCO OC AUTO MICRO 80 FOB TEST
K041297 POLYMEDCO OC LIGHT FOBT TEST
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