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

72 DETERMIN. SIZE RADIAL IMMUNOD. TEST

K Number: K811613 · Decision Aug 12, 1981
Classifications
1
FEI Numbers
33
Registration Numbers
33
Same Product Code
47
Applicant Total
40
Review Days
65

Basic Information

Device Name
72 DETERMIN. SIZE RADIAL IMMUNOD. TEST
K Number
K811613
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5880
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
KENT LABORATORIES, INC.
Date Received
June 8, 1981
Decision Date
August 12, 1981
Product Code
DDG
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
DDG Transferrin, Antigen, Antiserum, Control

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K950102 HUMAN C-5 RADIAL IMMUNODIFFUSION KIT
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K850690 ANTISERUM TO HUMAN APOLIPOPROTEIN B
K850686 ANTISERUM TO HUMAN PREALBUMIN
K831961 IMMUNODIFFUSION TEST HUMAN ANTITHROMBIN
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