AffloVest 8052
by Tactile Systems Technology Inc
AffloVest 8052 is a chest-percussion airway secretion-clearing system (FDA Class II; FDA product code BYI, Percussor, Powered-Electric) made by Tactile Systems Technology Inc, cleared under FDA 510(k) K122480 on 27 Mar 2013 and listed in FDA GUDID since 8 May 2022 (UDI-DI 00816305023732), 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 | Number00816305023732 | Date8 May 2022 | StatusListed |
| United States | FDA 510(k)SESE | NumberK122480 | Date27 Mar 2013 | StatusActive |
Official records
- AccessGUDID record 00816305023732
- FDA 510(k) database K122480
Across registries
- FDA 510(k) K122480 decided 27 Mar 2013 Active
- FDA GUDID UDI-DI 00816305023732 listed 8 May 2022 Listed
Timeline
- Cleared FDA 510(k) K122480
- Listed FDA GUDID 00816305023732
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- AffloVest
- Generic name
- Chest-percussion airway secretion-clearing system
- Model / reference
- 8052
- Primary DI / UDI-DI
- 00816305023732
- 510(k) Number
- FDA product code
- BYI
- GMDN term
- Chest-percussion airway secretion-clearing system
- Device class
- Class II
- Regulation number
- 868.5665
- GUDID distribution status
- In Commercial Distribution
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