Intl. Acoustics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Intl. Acoustics, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Intl. Acoustics, Inc. has 5 FDA 510(k) cleared medical devices. Based in Palatine, US.
Historical record: 5 cleared submissions from 1985 to 1987. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Intl. Acoustics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Intl. Acoustics, Inc.
5 devices
Cleared
Dec 07, 1987
MODIFIED DSP100 AMPLIFIER
Cardiovascular
89d
Cleared
Jun 10, 1987
DS-II DIGITAL SONOGRAPHY SYSTEM
Cardiovascular
223d
Cleared
May 12, 1987
DSP100 CAROTID PHONOANGIOGRAPHY MODULE
Cardiovascular
181d
Cleared
Dec 05, 1986
DSP100 AMPLIFIER
Cardiovascular
276d
Cleared
Apr 09, 1985
IAI PROGRAM-COMPUTER PROGRAM
Cardiovascular
104d