Relieva Spinplus RSP0616F
Relieva Spinplus RSP0616F is a Class I device made by Acclarent, Inc., cleared under FDA 510(k) K143541 on 22 Apr 2015 and listed in FDA GUDID since 1 Oct 2016 (UDI-DI 10705031232914), 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 | Number10705031232914 | Date1 Oct 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK143541 | Date22 Apr 2015 | StatusActive |
Official records
- AccessGUDID record 10705031232914
- FDA 510(k) database K143541
Across registries
- FDA 510(k) K143541 decided 22 Apr 2015 Active
- FDA GUDID UDI-DI 10705031232914 listed 1 Oct 2016 Listed
Timeline
- Cleared FDA 510(k) K143541
- Listed FDA GUDID 10705031232914
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Relieva Spinplus
- Generic name
- Nasal haemostatic balloon
- Model / Ref / Catalog
- RSP0616F
- Primary DI / UDI-DI
- 10705031232914
- 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.