FDA Registration
Active
🇺🇸 United States
Duotip-Test
Reg #: 1450391
·
FEI: 1450391
·
Expires 2025
Products
1
Proprietary Names
3
Establishment Types
1
Classifications
1
Registration Details
- Registration Name
- LINCOLN DIAGNOSTICS, INC.
- Registration Number
- 1450391
- FEI Number
- 1450391
- Status
- Active
- Expiry Year
- 2025
- Initial Importer
- No
- Address
- 240 E. HICKORY POINT RD.
- City
- DECATUR
- State
- IL
- ZIP
- 62526
- Country
- US
Regulatory Submissions
- 510(k) Number
- K941820
Owner / Operator
- Firm Name
- LINCOLN DIAGNOSTICS, INC.
- Operator Number
- 1450391
- Address
- 240 E. HICKORY POINT RD.
- City
- Decatur
- State
- IL
- Postal Code
- 62526
- Country
- US
Products
| Device Name | Product Code | Device Class | Medical Specialty | Exempt | Created |
|---|---|---|---|---|---|
| Allergen And Vaccine Delivery Needles | SCL | Class 2 | General Hospital | No | 2007-11-01 |
Proprietary Names
Duotip-Test
UniTest PC
Duotip-Test II
Establishment Types
Manufacture Medical Device