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

DETERM. SIZE 72 RADIAL HUMAN HAPTOGLOB

K Number: K831957 · Decision Jul 18, 1983
Classifications
1
FEI Numbers
32
Registration Numbers
32
Same Product Code
17
Applicant Total
40
Review Days
31

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Basic Information

Device Name
DETERM. SIZE 72 RADIAL HUMAN HAPTOGLOB
K Number
K831957
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5460
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
Kent Laboratories, Inc.
Date Received
June 17, 1983
Decision Date
July 18, 1983
Product Code
DAD
Advisory Committee
Immunology
Review Advisory Committee
CH
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DAD Haptoglobin, Antigen, Antiserum, Control

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Other Clearances by Kent Laboratories, Inc.

K Number Device Name
K951966 HUMAN PREALBUMIN RADIAL IMMUNODIFFUSION KIT
K951967 HUMAN C1 INACTIVATOR OR C-1 ESTERASE INHIBITOR RADIAL IMMUNODIFFUSION KIT
K951968 HUMAN C1Q RADIAL IMMUNODIFFUSION KIT
K950102 HUMAN C-5 RADIAL IMMUNODIFFUSION KIT
K850683 72 DETERM. SIZE RADIAL IMMUNODIFFUSION TEST ALPHA2
K850682 72 DETERM. SIZE RADIAL IMMUNO. TEST HUMAN CERULOPL
K850691 ANTISERUM TO HUMAN APOLIPOPROTEIN A-I
K850690 ANTISERUM TO HUMAN APOLIPOPROTEIN B
K850686 ANTISERUM TO HUMAN PREALBUMIN
K831961 IMMUNODIFFUSION TEST HUMAN ANTITHROMBIN
Search all 40 clearances from Kent Laboratories, Inc. →