Applied Optronics Corp. is one of 10775 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Applied Optronics Corp. - FDA 510(k) Cleared Devices
Recent clearances: AOC MEDICAL SYSTEM MODEL PHASE II 50 SURGICAL DIODE LASER SYSTEM, AOC MEDICAL SYSTEM MODEL PHASE II 25 SURGICAL DIODE LASER SYSTEM, APPLIED OPTRONICS MODEL AOC 5060 SURGFICAL DIODE LASER SYSTEM
4
Total
4
Cleared
0
Denied
Applied Optronics Corp. has 4 FDA 510(k) cleared medical devices. Based in South Plainfield, US.
Historical record: 4 cleared submissions from 1996 to 1996. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Applied Optronics Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Applied Optronics Corp.
4 devices
Cleared
Nov 01, 1996
AOC MEDICAL SYSTEM MODEL PHASE II 50 SURGICAL DIODE LASER SYSTEM
General & Plastic Surgery
183d
Cleared
Nov 01, 1996
AOC MEDICAL SYSTEM MODEL PHASE II 25 SURGICAL DIODE LASER SYSTEM
General & Plastic Surgery
183d
Cleared
Jan 26, 1996
APPLIED OPTRONICS MODEL AOC 5060 SURGFICAL DIODE LASER SYSTEM
General & Plastic Surgery
86d
Cleared
Jan 26, 1996
APPLIED OPTRONICS MODEL AOC 25 SURGICAL DIODE
General & Plastic Surgery
86d