Vortran Medical Technology 1, Inc. - FDA 510(k) Cleared Devices
28
Total
28
Cleared
0
Denied
Vortran Medical Technology 1, Inc. has 28 FDA 510(k) cleared anesthesiology devices. Based in Mchenry, US.
Last cleared in 2021. Active since 1984.
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 Vortran Medical Technology 1, Inc.
28 devices
Cleared
Feb 11, 2021
VORTRAN GO2VENT with PEEP Valve
Anesthesiology
189d
Cleared
Sep 18, 2019
VORTRAN APM-Plus
Anesthesiology
391d
Cleared
May 25, 2018
VORTRAN Cuff Inflator (VCI)
Anesthesiology
154d
Cleared
Apr 10, 2017
VORTRAN GO2VENT
Anesthesiology
168d
Cleared
Sep 16, 2016
VORTRAN Manometer
Anesthesiology
263d
Cleared
Sep 15, 2011
VORTRAN AIRWAY PRESSURE MONITOR (VAPM)-ADULT, VORTRAN AIRWAY PRESSURE MONITOR...
Anesthesiology
276d
Cleared
May 23, 2008
VAR MONITOR
Anesthesiology
185d
Cleared
Jul 15, 2004
VAR-PLUS (VORTRAN AUTOMATIC RESUSCITATOR), MODEL PCM
Anesthesiology
43d
Cleared
Feb 23, 2001
PERCUSSIVENEB, MODEL PN-2001
Anesthesiology
86d
Cleared
Jul 05, 2000
RESPIRTECH PRO-O2C, MODEL 2200 AND RESPIRTECH PRO, MODEL 2000
Anesthesiology
61d
Cleared
Nov 03, 1998
PIPER IPPB MODEL 2055
Anesthesiology
148d
Cleared
Sep 17, 1998
PERCUSSIVETECH HF, MODEL 2001
Anesthesiology
125d