Asico, LLC is one of 21679 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Asico, LLC - FDA 510(k) Cleared Devices
Recent clearances: ASICO SOFTIP INJECTOR SYSTEM, ROYALE AE 9036 LSP INJECTOR
2
Total
2
Cleared
0
Denied
Asico, LLC has 2 FDA 510(k) cleared medical devices. Based in Westmont, US.
Historical record: 2 cleared submissions from 2007 to 2011. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Asico, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Asico, LLC
2 devices