Endooptiks, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ENDO OPTIKS UROLOGICAL CATHETER FOR ENDOSCOPY, MODEL SESSR, MICROPROBE LASER AND ENDOSCOPY SYSTEM, MODEL E2
5
Total
5
Cleared
0
Denied
FDA 510(k) Regulatory Record - Endooptiks, Inc. General & Plastic Surgery ✕
3 devices