Cathworks, Ltd. is one of 267 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.
Cathworks, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: FFRangio, FFRangio System
2
Total
2
Cleared
0
Denied
Cathworks, Ltd. has 2 FDA 510(k) cleared medical devices. Based in Kfar-Saba, IL.
Historical record: 2 cleared submissions from 2018 to 2019. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Cathworks, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Heyer Regulatory Solutions, LLC as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Cathworks, Ltd.
2 devices