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

Zeus IFA ANA HEp-2 Test System, Zeus dIFine

K Number: K201956 · Decision Apr 29, 2022
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
109
Applicant Total
1
Review Days
654

Basic Information

Device Name
Zeus IFA ANA HEp-2 Test System, Zeus dIFine
K Number
K201956
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5100
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Zeus Scientific, Inc.
Date Received
July 14, 2020
Decision Date
April 29, 2022
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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