MagPro Accessories Acc for MagPro R20
MagPro Accessories Acc for MagPro R20 (9016B0441) is a Class II device made by Tonica Elektronik A/S, cleared under FDA 510(k) K170114 on 1 May 2017 and listed in FDA GUDID since 25 Nov 2022 (UDI-DI 05713484030290), active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number05713484030290 | Date25 Nov 2022 | StatusListed |
| United States | FDA 510(k)SESE | NumberK170114 | Date1 May 2017 | StatusActive |
Official records
- AccessGUDID record 05713484030290
- FDA 510(k) database K170114
Across registries
- FDA 510(k) K170114 decided 1 May 2017 Active
- FDA GUDID UDI-DI 05713484030290 listed 25 Nov 2022 Listed
Timeline
- Cleared FDA 510(k) K170114
- Listed FDA GUDID 05713484030290
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- MagPro Accessories
- Generic name
- Magnetic neural stimulation system
- Model / Ref / Catalog
- Acc for MagPro R20, 9016B0441
- Primary DI / UDI-DI
- 05713484030290
- 510(k) Number
- FDA product code
- OBP
- GMDN term
- Magnetic neural stimulation system
- Device class
- Class II
- Regulation number
- 882.5805
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Unsafe
Similar devices in this category
Other devices filed under Magnetic neural stimulation system.