Htl Strefa SA is one of 10 FDA 510(k) medical device manufacturers from Poland in the dataset, ranked by real submission volume.
Htl Strefa SA - FDA 510(k) Cleared Devices
Recent clearances: DropSafe Safety Pen Needles
1
Total
1
Cleared
0
Denied
Htl Strefa SA has 1 FDA 510(k) cleared medical devices. Based in Ozork?w, PL.
Last cleared in 2022. Active since 2022. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Htl Strefa SA Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Htl Strefa SA
1 devices