Interscope, Inc. is one of 25942 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
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, EndoRotor
4
Total
3
Cleared
1
Denied
Interscope, Inc. has 3 FDA 510(k) cleared medical devices. Based in Worchester, US.
Historical record: 3 cleared submissions from 2017 to 2019. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Interscope, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Icon Clinical Research, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Interscope, Inc.
4 devices
Not Cleared
Dec 23, 2020
EndoRotor Device
Gastroenterology & Urology
282d
Cleared
Dec 13, 2019
EndoRotor Console, EndoRotor Catheter, EndoRotor Specimen Trap, EndoRotor...
Ear, Nose, Throat
269d
Cleared
Jan 03, 2019
EndoRotor Console, EndoRotor Catheters, EndoRotor Specimen Trap, EndoRotor...
Gastroenterology & Urology
248d
Cleared
Apr 18, 2017
EndoRotor
Gastroenterology & Urology
95d