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

AFT SYSTEM PROFICIENCY TESTING PROGRAM

K Number: K820088 · Decision Jan 26, 1982
Classifications
1
FEI Numbers
11
Registration Numbers
11
Same Product Code
23
Applicant Total
41
Review Days
13

Basic Information

Device Name
AFT SYSTEM PROFICIENCY TESTING PROGRAM
K Number
K820088
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5660
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
CALBIOCHEM-BEHRING CORP.
Date Received
January 13, 1982
Decision Date
January 26, 1982
Product Code
DBL
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
DBL Multiple Autoantibodies, Indirect Immunofluorescent, Antigen, Control

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