Customed, Inc. - FDA 510(k) Cleared Devices
Recent clearances: FANFOLD DRAPE 41 X 57 PRODUCT NO. 900-633, RECORDER NO. 0633, GOWN POLY REINFORCED LARGE(PRODUCT NO.900-522)/(REORDER NO. 0522), SUCTION CATHETER TRAY PRODUCT NO. 900277
36
Total
26
Cleared
0
Denied
FDA 510(k) Regulatory Record - Customed, Inc. Obstetrics & Gynecology ✕
4 devices