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 | Device Class | Medical Specialty |
|---|---|---|---|
| DHN | Antinuclear Antibody, Indirect Immunofluorescent, Antigen, Control | FDA class 2 | Immunology |
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