Infrasonics Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Infrasonics Corp. - FDA 510(k) Cleared Devices
20
Total
19
Cleared
0
Denied
Infrasonics Corp. has 19 FDA 510(k) cleared anesthesiology devices. Based in Walker, US.
Historical record: 19 cleared submissions from 1984 to 1995.
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) Regulatory Record - Infrasonics Corp.
20 devices
Cleared
Dec 28, 1995
ADULT VENTILATOR
Anesthesiology
547d
Cleared
Sep 25, 1995
OXY/STAR LOW FLOW BLENDER
Anesthesiology
94d
Cleared
Oct 27, 1993
STAR BREATHING CIRCUITS
Anesthesiology
23d
Cleared
Dec 01, 1992
VENTILATOR ADULT STAR MODIFICATION
Anesthesiology
181d
Cleared
Oct 22, 1992
INFANT STAR SERIES 500
Anesthesiology
90d
Cleared
Aug 24, 1992
MODEL 105 VENTILATOR, MODIFICATION
Anesthesiology
89d
Cleared
Aug 03, 1992
AIR STAR
Anesthesiology
159d
Cleared
Jun 11, 1992
INFRASONICS VENTILATOR ADULT STAR, MODIFICATION
Anesthesiology
414d
Cleared
Jan 09, 1992
STAR SYNC, MODIFICATION
Anesthesiology
126d
Cleared
Jan 30, 1991
ADULT STAR, MODIFICATION
Anesthesiology
68d
Cleared
Nov 16, 1990
TRANSCUTANEOUS ELECTRONIC NERVE STIMULATOR
Neurology
346d
Cleared
Mar 16, 1990
MODIFIED STAR CALC
Anesthesiology
156d