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

RPR CARD TEST SYSTEM

K Number: K810658 · Decision Mar 31, 1981
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
30
Applicant Total
281
Review Days
20

Basic Information

Device Name
RPR CARD TEST SYSTEM
K Number
K810658
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3820
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
BECKMAN INSTRUMENTS, INC.
Date Received
March 11, 1981
Decision Date
March 31, 1981
Product Code
GMQ
Advisory Committee
Microbiology
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
GMQ Antigens, Nontreponemal, All

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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. →