A.R.C. Laser AG is one of 25917 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
A.R.C. Laser AG - FDA 510(k) Cleared Devices
Recent clearances: LASER PACK I, LASER PACK II, PHACO PACK I, PHACO PACK II, A.R.C. LOW BUBBLE TURBO NEEDLE, MODEL WE0106.5, O-LAS OPHTHALMIC PHOTODISRUPTOR
3
Total
3
Cleared
0
Denied
A.R.C. Laser AG has 3 FDA 510(k) cleared medical devices. Based in Salt Lake City, US.
Historical record: 3 cleared submissions from 2000 to 2001. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by A.R.C. Laser AG Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - A.R.C. Laser AG
3 devices