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

ANTITHYROID ANTIBODY IMMUNOFLUORESCENT

K Number: K810982 · Decision May 1, 1981
Classifications
1
FEI Numbers
35
Registration Numbers
35
Same Product Code
91
Applicant Total
12
Review Days
18

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Basic Information

Device Name
ANTITHYROID ANTIBODY IMMUNOFLUORESCENT
K Number
K810982
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5870
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
Immuno-Products Industries
Date Received
April 13, 1981
Decision Date
May 1, 1981
Product Code
JZO
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
JZO System, Test, Thyroid Autoantibody

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Other Clearances by Immuno-Products Industries

K Number Device Name
K853122 IMMUNO-PROD IND FLUORE TREPONE ANTIBODY ABSORPED
K852230 ANA/LITE-RL TEST SYSTEM
K852231 ANA/LITE-HEP-2 TEST SYSTEM
K843613 FLUORESCENT TREPONEMEL ANTIBODY-ABSORB
K831054 ANTINUCLEAR ANTIBODY TISSUE CULTURE SUB
K830652 ANTI N DNA-HCP
K821576 ANTINUCLEAR ANTIBODY SCREEN FLOURESC
K810984 ANTIMITOCHONDRIAL IMMUNOFLUORESCENT TEST
K810983 ANTISMOOTH MUSCLE ANTIBODY TEST SYS
K810985 ANTINUCLEAR ANTIBODY IMMUNOFLUORESCENT
Search all 12 clearances from Immuno-Products Industries →