# Pari Respiratory Equipment, Inc.

- Location (FDA's records): Midlothian, VA
- FDA decisions: 10 (2009–2025): 10 510(k) clearances
- Product codes: CAF (8), BWF (2)
- 510(k) review time since 2016: median 232 days, against 219 for FDA's reviews in the same codes and years (2 of 5 faster)
- Predicates its devices cite: 23 (5 its own); citations of its devices by later devices: 6 (5 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Pari Innovative Manufacturers, Inc.: 7 (https://510kreport.com/company/pari-innovative-manufacturers)
- Pari Holding Co.: 5 (https://510kreport.com/company/pari-holding)
- Bradstreet Clinical Research Assoc., Inc.: 2 (https://510kreport.com/company/bradstreet-clinical-research-assoc)
- Dhd Healthcare Corp.: 2 (https://510kreport.com/company/dhd-healthcare)
- Hudson Respiratory Care, Inc.: 1 (https://510kreport.com/company/hudson-respiratory-care)
- Profile Therapeutics Plc: 1 (https://510kreport.com/company/profile-therapeutics)

## Firms that cite its devices most
- Trudell Medical Intl.: 1 (https://510kreport.com/company/trudell-medical-intl)

## Its most-cited devices
- K112859: Erapid Nebulizer System (2012), cited by 2
- K092918: Pari Vios (2010), cited by 2
- K223840: eRapid Nebulizer System (2023), cited by 1
- K100380: Altera Nebulizer System, Model 678G1002 (2010), cited by 1

## Recent decisions
- K251572: eRapid with eTrack System (Dec 19, 2025)
- K223840: eRapid Nebulizer System (Aug 11, 2023)
- K191270: Proneb Max (Jan 23, 2020)
- K162785: Velox Nebulizer System (Apr 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 (Feb 22, 2010)

Source page: https://510kreport.com/company/pari-respiratory-equipment