FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

HUMAN ALPHA, ACID GLYCOPROTEIN

K Number: K791341 · Decision Aug 16, 1979
Classifications
1
FEI Numbers
1
Registration Numbers
1
Same Product Code
4
Applicant Total
281
Review Days
31

Basic Information

Device Name
HUMAN ALPHA, ACID GLYCOPROTEIN
K Number
K791341
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.5420
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
BECKMAN INSTRUMENTS, INC.
Date Received
July 16, 1979
Decision Date
August 16, 1979
Product Code
DEX
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
DEX Alpha-1-B-Glycoprotein, Antigen, Antiserum, Control

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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. →