Pari Respiratory Equipment, Inc. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Pari Respiratory Equipment, Inc. has 10 FDA 510(k) cleared anesthesiology devices. Based in Midlothian, US.
Latest FDA clearance: Dec 2025. Active since 2009.
Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Pari Respiratory Equipment, Inc.
10 devices
Cleared
Dec 19, 2025
eRapid with eTrack System
Anesthesiology
211d
Cleared
Aug 11, 2023
eRapid Nebulizer System
Anesthesiology
232d
Cleared
Jan 23, 2020
Proneb Max
Anesthesiology
255d
Cleared
Apr 14, 2017
Velox Nebulizer System
Anesthesiology
193d
Cleared
May 27, 2016
O-PEP
Anesthesiology
501d
Cleared
May 30, 2012
ERAPID NEBULIZER SYSTEM
Anesthesiology
243d
Cleared
May 06, 2010
PARI SINUS
Anesthesiology
259d
Cleared
Feb 22, 2010
ALTERA NEBULIZER SYSTEM, MODEL 678G1002
Anesthesiology
6d
Cleared
Feb 04, 2010
PARI VIOS
Anesthesiology
135d
Cleared
Jul 21, 2009
PARI PEP S
Anesthesiology
117d