FDA Registration
Active
🇺🇸 United States
Quickloop Abscess Treatment Device
Reg #: 3018387313
·
FEI: 3018387313
·
Expires 2025
Products
1
Proprietary Names
1
Establishment Types
2
Classifications
1
Registration Details
- Registration Name
- EM DEVICE LAB, INC.
- Registration Number
- 3018387313
- FEI Number
- 3018387313
- Status
- Active
- Expiry Year
- 2025
- Initial Importer
- No
- Address
- 6303 Mountain Park Cv
- City
- Austin
- State
- TX
- ZIP
- 78731
- Country
- US
Owner / Operator
- Firm Name
- EM Device Lab, Inc.
- Operator Number
- 10081242
- Address
- 6303 Mountain Park Cv
- City
- Austin
- State
- TX
- Postal Code
- 78731
- Country
- US
- Correspondent
- Elisa Maldonado-Holmertz
Products
| Device Name | Product Code | Device Class | Medical Specialty | Exempt | Created |
|---|---|---|---|---|---|
| Catheter, Irrigation | GBX | Class 1 | General, Plastic Surgery | No | 2021-04-13 |
Proprietary Names
Quickloop Abscess Treatment Device
Establishment Types
Develop Specifications But Do Not Manufacture At This Facility
Manufacture Medical Device