Bypass , Ltd. is one of 25837 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Bypass , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: MODIFICATION TO CORLINK AUTOMATED ANASTOMOTIC DEVICE, CORLINK AAD (3.5 TO 6.0 M M OUTER DIAMETER VESSELS),MODEL 200-064, CORLINK AAD (2.0 TO 4.0 MM OUTER DIAMETER VESSELS), M
2
Total
2
Cleared
0
Denied
Bypass , Ltd. has 2 FDA 510(k) cleared medical devices. Based in Washington, US.
Historical record: 2 cleared submissions from 2001 to 2002. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Bypass , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Bypass , Ltd.
2 devices