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

RHEUMELISA II HISTONE ANTIBODY TEST KIT

K Number: K932679 · Decision Aug 23, 1993
Classifications
1
FEI Numbers
18
Registration Numbers
18
Same Product Code
49
Applicant Total
10
Review Days
82

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Basic Information

Device Name
RHEUMELISA II HISTONE ANTIBODY TEST KIT
K Number
K932679
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5100
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Biowhittaker Molecular Applications, Inc.
Date Received
June 2, 1993
Decision Date
August 23, 1993
Product Code
LKJ
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
LKJ Antinuclear Antibody, Antigen, Control

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K925209 MUMPS STAT
K935618 SPECIMEN TRANSPORT MEDIUM
K930757 RHEUMELISA II JO-1 ANTIBODY TEST KIT
K930130 RHEUMELISA II SCL-70 ANTIBODY TEST KIT
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