Relieva Spin RSF70Z
Relieva Spin RSF70Z is a Class I device made by Acclarent, Inc., cleared under FDA 510(k) K111875 on 11 Oct 2011 and listed in FDA GUDID since 1 Oct 2016 (UDI-DI 20705031200538), active as of 23 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 | Number20705031200538 | Date1 Oct 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK111875 | Date11 Oct 2011 | StatusActive |
Official records
- AccessGUDID record 20705031200538
- FDA 510(k) database K111875
Across registries
- FDA 510(k) K111875 decided 11 Oct 2011 Active
- FDA GUDID UDI-DI 20705031200538 listed 1 Oct 2016 Listed
Timeline
- Cleared FDA 510(k) K111875
- Listed FDA GUDID 20705031200538
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Relieva Spin
- Generic name
- Nasal haemostatic balloon
- Model / Ref / Catalog
- RSF70Z
- Primary DI / UDI-DI
- 20705031200538
- 510(k) Number
- FDA product code
- LRC
- GMDN term
- Nasal haemostatic balloon
- Device class
- Class I
- Regulation number
- 874.4420
- GUDID distribution status
- In Commercial Distribution
Similar devices in this category
Other devices filed under Nasal haemostatic balloon.