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

BION ANTINUCLEAR ANTIBODY(ANA)TEST KIT/CONTR SERUM

K Number: K872845 · Decision Aug 17, 1987
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
109
Applicant Total
14
Review Days
28

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Basic Information

Device Name
BION ANTINUCLEAR ANTIBODY(ANA)TEST KIT/CONTR SERUM
K Number
K872845
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5100
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
Bion Ent., Ltd.
Date Received
July 20, 1987
Decision Date
August 17, 1987
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (DHN), ordered by most recent decision date.

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Other Clearances by Bion Ent., Ltd.

K Number Device Name
K926066 BION MUMPS-G ANTIBODY TEST SYSTEM
K901054 BION BORRELIA BURGDORFERI ANTIGEN SUBSTRATE SLIDE
K894622 VARICELLA ZOSTER VIRUS
K894624 MUMPS VIRUS
K894623 RESPIRATORY SYNCYTIAL VIRUS
K894626 EPSTEIN-BARR VIRUS-NUCLEAR ANTIGEN
K891785 BION EBV-G (VCA) TEST SYSTEM
K894625 CHLAMYDIA (LGV-1)
K893240 BION EBV-M (VCA) TEST SYSTEM
K890616 BION DIRECT IDENTIFICATION CONTROL SLIDE
Search all 14 clearances from Bion Ent., Ltd. →