V7 plus b emergency
by Hersill Sl
V7 plus b emergency (5320222) is an emergency airway clearance suction system (FDA Class II; FDA product code BTA, Pump, Portable, Aspiration (Manual Or Powered)) made by Hersill Sl, cleared under FDA 510(k) K093241 on 27 Apr 2010 and listed in FDA GUDID since 21 Sep 2018 (UDI-DI 08435331771305), 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 | Number08435331771305 | Date21 Sep 2018 | StatusListed |
| United States | FDA 510(k)SESE | NumberK093241 | Date27 Apr 2010 | StatusActive |
Official records
- AccessGUDID record 08435331771305
- FDA 510(k) database K093241
Across registries
- FDA 510(k) K093241 decided 27 Apr 2010 Active
- FDA GUDID UDI-DI 08435331771305 listed 21 Sep 2018 Listed
Timeline
- Cleared FDA 510(k) K093241
- Listed FDA GUDID 08435331771305
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- V7
- Generic name
- Emergency airway clearance suction system, electric
- Model / Ref / Catalog
- V7 plus b emergency, 5320222
- Primary DI / UDI-DI
- 08435331771305
- 510(k) Number
- FDA product code
- BTA
- GMDN term
- Emergency airway clearance suction system, electric
- Device class
- Class II
- Regulation number
- 878.4780
- GUDID distribution status
- In Commercial Distribution
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