FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
ANA SCREEN ELISA TEST SYSTEM
K Number: K940362
·
Decision Jul 28, 1994
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
179
Applicant Total
135
Review Days
183
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Basic Information
- Device Name
- ANA SCREEN ELISA TEST SYSTEM
- K Number
- K940362
- 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
- January 26, 1994
- Decision Date
- July 28, 1994
- Product Code
- LLL
- 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 |
|---|---|---|---|
| LLL | Extractable Antinuclear Antibody, Antigen And Control | FDA class 2 | Immunology |
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