Naser Dib Gabinet Lekarksi Nasmed is one of 10 FDA 510(k) medical device manufacturers from Poland in the dataset, ranked by real submission volume.
Naser Dib Gabinet Lekarksi Nasmed - FDA 510(k) Cleared Devices
Recent clearances: Gastric Lightguide (GLG)
1
Total
1
Cleared
0
Denied
Naser Dib Gabinet Lekarksi Nasmed has 1 FDA 510(k) cleared medical devices. Based in Warszawa, PL.
Last cleared in 2022. Active since 2022. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Naser Dib Gabinet Lekarksi Nasmed Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Aztech Regulatory & Quality, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Naser Dib Gabinet Lekarksi Nasmed
1 devices