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

ANA SENSITIVITY/SPECIFICITY CONTROL

K Number: K841776 · Decision Jun 22, 1984
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
109
Applicant Total
145
Review Days
53

Basic Information

Device Name
ANA SENSITIVITY/SPECIFICITY CONTROL
K Number
K841776
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5100
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
BEHRING DIAGNOSTICS, INC.
Date Received
April 30, 1984
Decision Date
June 22, 1984
Product Code
DHN
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
DHN Antinuclear Antibody, Indirect Immunofluorescent, Antigen, Control

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