Pathway, LLC is one of 25960 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pathway, LLC - FDA 510(k) Cleared Devices
Recent clearances: HDX 100% Silicone 2-way Foley Catheter, 14Fr/10cc, HDX 100% Silicone 2-way Foley Catheter, 16Fr/5cc, HDX 100% Silicone 2-way Foley Catheter, 18Fr/10cc, PSM 3-Way Silicone Foley Catheter, Kurin Blood Culture Collection Set
3
Total
3
Cleared
0
Denied
Pathway, LLC has 3 FDA 510(k) cleared medical devices. Based in Santee, US.
Historical record: 3 cleared submissions from 2016 to 2020. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Pathway, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Pathway, LLC
3 devices