Impact Instrumentation, Inc. - FDA 510(k) Cleared Devices
27
Total
27
Cleared
0
Denied
Impact Instrumentation, Inc. has 27 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 27 cleared submissions from 1981 to 2014. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Impact Instrumentation, Inc. Filter by specialty or product code using the sidebar.
27 devices
Cleared
Mar 10, 2014
IMPACT MODEL 323 ASPIRATOR
General & Plastic Surgery
144d
Cleared
Feb 16, 2012
UNI-VENT (R) MODEL 731 SERIES PORTABLE CRITICAL CARE VENTILATOR
Anesthesiology
265d
Cleared
Apr 07, 2011
UNI-VENT 731 SERIES MODEL EMV+ PORTABLE CRITICAL CARE VENTILATOR
Anesthesiology
146d
Cleared
Aug 13, 2009
UNI-VENT-731 SERIES VENTILATORS, MODEL 731EMV+
Anesthesiology
108d
Cleared
Dec 10, 2008
UNI-VENT 731 SERIES VENTILATORS, MODEL 731, 731EMV
Anesthesiology
555d
Cleared
Oct 28, 2005
UNI-VENT MODEL 73X
Anesthesiology
147d
Cleared
Mar 26, 2004
UNI-VENT MODEL 730AEV (AUTOMATIC EMERGENCY VENTILATOR)
Anesthesiology
235d
Cleared
May 06, 2003
IMPACT, UNIVERSAL SINGLE-LIMB, VENTILATOR CIRCUIT, MODEL 820-0099-00
Anesthesiology
315d
Cleared
Apr 18, 1995
ASPIRATOR, CONTINUOUS & PROGRAMMABLE INTERMITTENT
General & Plastic Surgery
22d
Cleared
Jan 05, 1995
ELECTRIC VACUM PUMP
General & Plastic Surgery
304d
Cleared
Dec 30, 1994
IMPACT MODEL 753
Anesthesiology
646d
Cleared
Dec 27, 1990
POWERED VENTILATOR, LEVER I/II, BATTLEFIELD USE
Anesthesiology
3d