Interscope, Inc. - FDA 510(k) Cleared Devices
Recent clearances: EndoRotor Console, EndoRotor Catheter, EndoRotor Specimen Trap, EndoRotor Filter Set, EndoRotor Roll Stand, EndoRotor Console, EndoRotor Catheters, EndoRotor Specimen Trap, EndoRotor Filter Set, EndoRotor Foot Control
4
Total
3
Cleared
1
Denied
FDA 510(k) Regulatory Record - Interscope, Inc. Ear, Nose, Throat ✕
1 devices