Pari Respiratory Equipment, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 10
- Inspections
- 4
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K251572 | eRapid with eTrack System | December 19, 2025 |
| K223840 | eRapid Nebulizer System | August 11, 2023 |
| K191270 | Proneb Max | January 23, 2020 |
| K162785 | Velox Nebulizer System | April 14, 2017 |
| K150044 | O-PEP | May 27, 2016 |
| K112859 | ERAPID NEBULIZER SYSTEM | May 30, 2012 |
| K092560 | PARI SINUS | May 6, 2010 |
| K100380 | ALTERA NEBULIZER SYSTEM, MODEL 678G1002 | February 22, 2010 |
| K092918 | PARI VIOS | February 4, 2010 |
| K090829 | PARI PEP S | July 21, 2009 |