FDA Registration
Active
🇺🇸 United States
LiquID 6F Guide Catheter Extension
Reg #: 3017708755
·
FEI: 3017708755
·
Expires 2025
Products
1
Proprietary Names
2
Establishment Types
1
Classifications
1
Registration Details
- Registration Name
- SEIGLA MEDICAL, INC.
- Registration Number
- 3017708755
- FEI Number
- 3017708755
- Status
- Active
- Expiry Year
- 2025
- Initial Importer
- No
- Address
- 7688 5th Street SE
- City
- Buffalo
- State
- MN
- ZIP
- 55313
- Country
- US
Regulatory Submissions
- 510(k) Number
- K220691
Owner / Operator
- Firm Name
- Seigla Medical, Inc.
- Operator Number
- 10083573
- Address
- 7688 5th Street SE
- City
- Buffalo
- State
- MN
- Postal Code
- 55313
- Country
- US
- Correspondent
- Craig R Schlawin
Products
| Device Name | Product Code | Device Class | Medical Specialty | Exempt | Created |
|---|---|---|---|---|---|
| Catheter, Percutaneous | DQY | Class 2 | Cardiovascular | No | 2022-11-02 |
Proprietary Names
LiquID 6F Guide Catheter Extension
LiquID 7F Guide Catheter Extension
Establishment Types
Manufacture Medical Device