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

RHEUMATOID FACTOR REAGENT TEST KIT

K Number: K810306 · Decision Mar 11, 1981
Classifications
1
FEI Numbers
57
Registration Numbers
57
Same Product Code
143
Applicant Total
281
Review Days
34

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Basic Information

Device Name
RHEUMATOID FACTOR REAGENT TEST KIT
K Number
K810306
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5775
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
Beckman Instruments, Inc.
Date Received
February 5, 1981
Decision Date
March 11, 1981
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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Other Clearances by Beckman Instruments, Inc.

K Number Device Name
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K982250 ACCESS FREE T4 REAGENTS ON THE ACCESS IMMUNOASSAY ANALYZER
K981403 IMMAGE IMMUNOCHEMISTRY SYSTEM VALPROIC ACID (VPA) REAGENT
K981354 ACCESS AFP REAGENTS ON THE ACCESS IMMUNOASSAY ANALYZER MODEL NUMBER 33211
K980173 ACCESS TOTAL BHCG REAGENTS ON THE ACCESS IMMUNOASSAY ANALYZER; 33500, 33505
K974816 ACCESS(R) PSA REAGENTS ON THE ACCESS(R) IMMUNOASSAY ANALYZER 33220, 33225, 33229
K974564 IMMAGE IMMUNOCHEMISTRY SYSTEM ALPHA-2-MACROGLOBULIN REAGENT
K974110 IMMAGE IMMUNOCHEMISTRY SYSTEM ANTITHROMBIN III (AT3) REAGENT
K974452 VIGIL LIPID CONTROL
K973932 BECKMAN CALIBRATOR 2 (CAL2)
Search all 281 clearances from Beckman Instruments, Inc. →