Vortex 051F5210
by Pari Respiratory Equipment, Inc.
Vortex 051F5210 is a Class II device made by Pari Respiratory Equipment, Inc., cleared under FDA 510(k) K020944 on 9 May 2002 and listed in FDA GUDID since 15 Aug 2016 (UDI-DI 00744229510239), 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 | Number00744229510239 | Date15 Aug 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK020944 | Date9 May 2002 | StatusActive |
Official records
- AccessGUDID record 00744229510239
- FDA 510(k) database K020944
Across registries
- FDA 510(k) K020944 decided 9 May 2002 Active
- FDA GUDID UDI-DI 00744229510239 listed 15 Aug 2016 Listed
Timeline
- Cleared FDA 510(k) K020944
- Listed FDA GUDID 00744229510239
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Vortex
- Generic name
- Medicine chamber spacer, reusable
- Model / reference
- 051F5210
- Primary DI / UDI-DI
- 00744229510239
- 510(k) Number
- FDA product code
- CAF
- GMDN term
- Medicine chamber spacer, reusable
- Device class
- Class II
- Regulation number
- 868.5630
- GUDID distribution status
- In Commercial Distribution
Similar devices
Other devices filed under FDA product code CAF (Nebulizer (Direct Patient Interface)).
- Hailie Sensor by Adherium (Nz), Ltd.
- FindAir ONE for pMDI (FAO-MDI-V12-GRE-001) by FindAir Sp. z o. o.
- Airworks Nebulizer pe1200m by Convexity Scientific, LLC
- MiniSpacer Dual Spray MDI Adapter 1024, 1025, 1543, 1024A, 1025A, 1543A by THAYER MEDICAL CORPORATION
- 0.9% SODIUM CHLORIDE SOL./RESP. THERAPY by Abbott Laboratories
- OMRON COMPRESSOR SYSTEMS, MODELS NE-C28, NE-C30 by Omron Healthcare, Inc.
- MICRO-MISTER by Bp, Ltd.
- OMRON COMPRESSOR NEBULIZER- MODEL NE-C09 by Omron Healthcare, Inc.
- Hudson RCI AddiPak Unit Dose Vial by MEDLINE INDUSTRIES, INC.
- PREEMICARE NEBUTECH NEBULIZER SYSTEM by Preemicare Corp.