Aircast, Inc. is one of 14768 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Aircast, Inc. - FDA 510(k) Cleared Devices
Recent clearances: VENAFLOW SYSTEM, MODEL 30A, AIRCAST VENA FLOW STERILE DISPOSABLE CUFFS, AIRCAST VENAFLOW SYSTEM (MODIFICATION)
11
Total
11
Cleared
0
Denied
Aircast, Inc. has 11 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 11 cleared submissions from 1978 to 2003. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Aircast, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Aircast, Inc.
11 devices
Cleared
Jun 03, 2003
ARTERIALFLOW SYSTEM, MODEL 32A
Cardiovascular
180d
Cleared
Feb 10, 2003
VENAFLOW REUSABLE CALF AIRCELL, MODEL 3018, VENAFLOW DISPOSABLE CALF COVER,...
Cardiovascular
88d
Cleared
Jan 13, 2000
VENAFLOW SYSTEM, MODEL 30A
Cardiovascular
174d
Cleared
Sep 08, 1997
AIRCAST VENA FLOW STERILE DISPOSABLE CUFFS
Cardiovascular
320d
Cleared
Mar 28, 1997
AIRCAST VENAFLOW SYSTEM (MODIFICATION)
Cardiovascular
350d
Cleared
Dec 07, 1993
AIRCAST EDEMAFLOW SYSTEM
Cardiovascular
116d
Cleared
Oct 25, 1993
AIRCAST VENAFLOW SYSTEM
Cardiovascular
133d
Cleared
Apr 14, 1993
AUTOCHILL ACCESSORY KIT
Physical Medicine
272d
Cleared
Aug 13, 1981
AIRCAST PNEUMATIC KNEE BRACE
Physical Medicine
20d
Cleared
Feb 12, 1981
AIRCAST TENNIS ARM BAND
Physical Medicine
10d
Cleared
Jun 30, 1978
AIRSTIRRUP PNEUMATIC ANKLE BRACE
Physical Medicine
21d