M. Imonti and Associates Inc., - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
M. Imonti and Associates Inc., has 6 FDA 510(k) cleared medical devices. Based in San Juan Capistrano, US.
Historical record: 6 cleared submissions from 1991 to 1995. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by M. Imonti and Associates Inc., Filter by specialty or product code using the sidebar.
6 devices
Cleared
May 22, 1995
PRO-PAK FOR OMS DIPLOMATE
Ophthalmic
90d
Cleared
Apr 28, 1995
PRO-VIT
Ophthalmic
66d
Cleared
Jan 25, 1994
PHACOFRAGMENTOR TIP
Ophthalmic
182d
Cleared
Jan 06, 1994
PRO-PHACO HANDPIECE
Ophthalmic
171d
Cleared
Dec 08, 1992
ENDO TRACHEA TUBE FIXATION
Anesthesiology
90d
Cleared
Mar 06, 1991
DRAINAGE TUBE RESTRAINT/WOUND COVER
General & Plastic Surgery
69d