Pari Innovative Manufacturers, Inc. is one of 25192 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pari Innovative Manufacturers, Inc. - FDA 510(k) Cleared Devices
Recent clearances: MODIFICATION TO: EFLOW ELECTRONIC INHALER/NEBULIZER, PARI HYDRATE V, HYPER SAL
10
Total
10
Cleared
0
Denied
Pari Innovative Manufacturers, Inc. has 10 FDA 510(k) cleared anesthesiology devices. Based in Midlothian, US.
Historical record: 10 cleared submissions from 2002 to 2007.
Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Citech and Intertek Testing Services.
FDA 510(k) Regulatory Record - Pari Innovative Manufacturers, Inc.
10 devices
Cleared
Dec 13, 2007
MODIFICATION TO: EFLOW ELECTRONIC INHALER/NEBULIZER
Anesthesiology
83d
Cleared
Nov 29, 2007
PARI HYDRATE V
Anesthesiology
37d
Cleared
Apr 26, 2007
HYPER SAL
Anesthesiology
65d
Cleared
Feb 23, 2007
PARI HYDRATE G
Anesthesiology
43d
Cleared
Aug 28, 2006
LC SPRINT STAR
Anesthesiology
31d
Cleared
Jun 02, 2006
LC STAR WITH NASAL ADAPTER
Anesthesiology
15d
Cleared
Apr 05, 2006
TREK S NEBULIZER COMPRESSOR
Anesthesiology
51d
Cleared
Mar 02, 2006
LC SPRINT NEBULIZER
Anesthesiology
15d
Cleared
May 05, 2004
EFLOW ELECTRONIC INHALER/NEBULIZER
Anesthesiology
147d
Cleared
May 09, 2002
VORTEX VALVED HOLDING CHAMBER
Anesthesiology
45d