Aros Surgical Instruments Corporation is one of 18413 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Aros Surgical Instruments Corporation - FDA 510(k) Cleared Devices
Recent clearances: Vein Clamps, Artery Clamps
1
Total
1
Cleared
0
Denied
Aros Surgical Instruments Corporation has 1 FDA 510(k) cleared medical devices. Based in Newport Beach, US.
Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Aros Surgical Instruments Corporation Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Specialist, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Aros Surgical Instruments Corporation
1 devices