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

CRITHIDIA LUCILIAE NATIVE DNA-IFA TEST

K Number: K810301 · Decision Feb 25, 1981
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
109
Applicant Total
36
Review Days
21

Basic Information

Device Name
CRITHIDIA LUCILIAE NATIVE DNA-IFA TEST
K Number
K810301
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5100
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
IMMUNO CONCEPTS, INC.
Date Received
February 4, 1981
Decision Date
February 25, 1981
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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