Newport Medical Instruments, Inc. - FDA 510(k) Cleared Devices
22
Total
19
Cleared
0
Denied
Newport Medical Instruments, Inc. has 19 FDA 510(k) cleared anesthesiology devices. Based in Mchenry, US.
Historical record: 19 cleared submissions from 1982 to 2012.
Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
22 devices
Cleared
Nov 09, 2012
NEWPORT AURA VENTILATOR
Anesthesiology
133d
Cleared
Dec 01, 2011
NEWPORT HT70 VENTILATOR
Anesthesiology
223d
Cleared
Sep 08, 2010
NEWPORT E360 VENTILATOR
Anesthesiology
72d
Cleared
Nov 18, 2009
NEWPORT HT70 FAMILY OF VENTILATORS
Anesthesiology
232d
Cleared
Dec 16, 2008
NEWPORT HTS50 VENTILATOR WITH DUAL PAC BATTERY SYSTEM
Anesthesiology
90d
Cleared
Jul 28, 2006
NEWPORT E500 WAVE VENTILATOR
Anesthesiology
100d
Cleared
Jan 10, 2006
NEWPORT E360 VENTILATOR
Anesthesiology
25d
Cleared
Sep 07, 2004
NEWPORT NEBSONIC N550 ULTRASONIC NEBULIZER
Anesthesiology
134d
Cleared
Jan 23, 2004
NEWPORT E500 WAVE VENTILATOR
Anesthesiology
318d
Cleared
Aug 04, 2000
NEWPORT HT50 VENTILATOR WITH HUMIDIFIER HT50-H, NEWPORT HT50 VENTILATOR...
Anesthesiology
408d
Cleared
Sep 23, 1999
E100M VENTILATOR (E100M)
Anesthesiology
785d
Cleared
Aug 25, 1995
NEWPORT ELECTRONIC MANOMETER
Anesthesiology
536d