Feliks Plastik Laminasyon VE Ambalaj Malzemeleri Sanayi - FDA 510(k) ...
2
Total
2
Cleared
0
Denied
Feliks Plastik Laminasyon VE Ambalaj Malzemeleri Sanayi has 2 FDA 510(k) cleared medical devices. Based in Eskisehir, TR.
Last cleared in 2022. Active since 2022. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Feliks Plastik Laminasyon VE Ambalaj Malzemeleri Sanayi Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Dp Distribution & Consulting, LLC and Rogers Consulting.
FDA 510(k) Regulatory Record - Feliks Plastik Laminasyon VE Ambalaj Malzemeleri Sanayi
2 devices