Impact Instrumentation, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Impact Instrumentation, Inc. - FDA 510(k) Cleared Devices
Recent clearances: IMPACT MODEL 323 ASPIRATOR, UNI-VENT (R) MODEL 731 SERIES PORTABLE CRITICAL CARE VENTILATOR, UNI-VENT 731 SERIES MODEL EMV+ PORTABLE CRITICAL CARE VENTILATOR
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.
FDA 510(k) Regulatory Record - Impact Instrumentation, Inc.
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