Propeller Sensor Model 2014-R
Propeller Sensor Model 2014-R is an inhaler dose sensor (FDA Class II; FDA product code CAF, Nebulizer (Direct Patient Interface)) made by Reciprocal Labs, cleared under FDA 510(k) K142960 on 5 Mar 2015 and listed in FDA GUDID since 22 Jul 2016 (UDI-DI 00865528000020), 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 | Number00865528000020 | Date22 Jul 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK142960 | Date5 Mar 2015 | StatusActive |
Official records
- AccessGUDID record 00865528000020
- FDA 510(k) database K142960
Across registries
- FDA 510(k) K142960 decided 5 Mar 2015 Active
- FDA GUDID UDI-DI 00865528000020 listed 22 Jul 2016 Listed
Timeline
- Cleared FDA 510(k) K142960
- Listed FDA GUDID 00865528000020
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Propeller
- Generic name
- Inhaler dose sensor
- Model / reference
- Sensor Model 2014-R
- Primary DI / UDI-DI
- 00865528000020
- 510(k) Number
- FDA product code
- CAF
- GMDN term
- Inhaler dose sensor
- Device class
- Class II
- Regulation number
- 868.5630
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Unsafe
Similar devices
Other devices filed under FDA product code CAF (Nebulizer (Direct Patient Interface)).
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