Randwal Instrument Co., Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Randwal Instrument Co., Inc. has 6 FDA 510(k) cleared medical devices. Based in Southbridge, US.
Historical record: 6 cleared submissions from 1983 to 1988. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Randwal Instrument Co., Inc. Filter by specialty or product code using the sidebar.
6 devices
Cleared
Feb 05, 1988
IRAS EDS INTERFEROMETRIC STIMULATOR
Ophthalmic
127d
Cleared
Nov 24, 1987
IRAS GLARE TESTER
Ophthalmic
56d
Cleared
Dec 12, 1986
IRAS PERIMETER
Ophthalmic
58d
Cleared
Nov 01, 1985
LASER IRAS
Ophthalmic
67d
Cleared
Aug 15, 1984
PORTABLE ACUIOMETER
Ophthalmic
44d
Cleared
Jan 24, 1983
VARIABLE CONTRAST ACUIOMETER, DIAGNOSTIC LASER INTERFEROMETER
Radiology
35d