SmartVest CLEARWAY-PED
SmartVest CLEARWAY-PED is a Class II device made by Electromed, Inc., cleared under FDA 510(k) K222496 on 18 Nov 2022 and listed in FDA GUDID since 5 Jul 2023 (UDI-DI B102125011S0100), 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 | NumberB102125011S0100 | Date5 Jul 2023 | StatusListed |
| United States | FDA 510(k)SESE | NumberK222496 | Date18 Nov 2022 | StatusActive |
Official records
- FDA 510(k) database K222496
Across registries
- FDA 510(k) K222496 decided 18 Nov 2022 Active
- FDA GUDID UDI-DI B102125011S0100 listed 5 Jul 2023 Listed
Timeline
- Cleared FDA 510(k) K222496
- Listed FDA GUDID B102125011S0100
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- SmartVest
- Generic name
- Chest-oscillation airway secretion-clearing system generator
- Model / Ref / Catalog
- CLEARWAY-PED
- Primary DI / UDI-DI
- B102125011S0100
- 510(k) Number
- FDA product code
- BYI
- GMDN term
- Chest-oscillation airway secretion-clearing system generator
- Device class
- Class II
- Regulation number
- 868.5665
- GUDID distribution status
- In Commercial Distribution
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