Laser Industries , Ltd. - FDA 510(k) Cleared Devices
20
Total
20
Cleared
0
Denied
Laser Industries , Ltd. has 20 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 20 cleared submissions from 1978 to 1994. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Laser Industries , Ltd. Filter by specialty or product code using the sidebar.
20 devices
Cleared
Apr 07, 1994
SHARPLAN CO2 SURGICAL LASER
General & Plastic Surgery
272d
Cleared
Sep 28, 1989
SHARPLAN SMOKE EVACUATION UNIT, MODEL 100
General Hospital
64d
Cleared
Aug 07, 1985
SHARPLAN 1040 CO/2 SURGICAL LASER
General & Plastic Surgery
169d
Cleared
Aug 07, 1985
SHARPLAN MODEL 1060 CO/2 SURGICAL LASER
General & Plastic Surgery
169d
Cleared
Aug 27, 1984
LASER RECTOSCOPE SET 784
Gastroenterology & Urology
28d
Cleared
Apr 25, 1984
SHARPLAN #734 LASER SURGICAL UNIT
General & Plastic Surgery
268d
Cleared
Apr 23, 1984
SHARPLAN #745 LASER SURG. UNIT
General & Plastic Surgery
266d
Cleared
Jan 30, 1984
OPHTHALMIC ARGON LASER #700A
Ophthalmic
199d
Cleared
Jun 28, 1983
SHARPLAN LASER POSITIONING SYSTEM
Radiology
32d
Cleared
May 18, 1983
SHARPLAN 721 CO2 SURGICAL LASER
Radiology
71d
Cleared
Mar 09, 1983
MICROSCAN 771 MANIPULATOR
Radiology
43d
Cleared
Jan 06, 1983
MODEL 716 MICROMANIPULATOR
Radiology
31d