Icor AB - FDA 510(k) Cleared Devices
Recent clearances: ET-TUBE PLACEMENT DETECTOR (WITH COLIBRI INDICATOR), TYPE 1 & 2 (HUMIDAIR I & II), ET TUBE PLACEMENT DETECTOR (WITH COLIBRI INDICATOR)
16
Total
16
Cleared
0
Denied
FDA 510(k) Regulatory Record - Icor AB Ophthalmic ✕
1 devices