Turboseal, L.P. is one of 472 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.
Turboseal, L.P. - FDA 510(k) Cleared Devices
Recent clearances: TurboSEAL Nasogastric Aspiration Tube
1
Total
1
Cleared
0
Denied
Turboseal, L.P. has 1 FDA 510(k) cleared medical devices. Based in Tel Aviv, IL.
Historical record: 1 cleared submissions from 2014 to 2014. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Turboseal, L.P. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Dohmen Life Science Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Turboseal, L.P.
1 devices