EndoRotor Device— 510(k) DEN200016

Unknown

Interscope, Inc.

FDA 510(k) clearance DEN200016 for EndoRotor Device, Unknown on 2020-12-23. Applicant: Interscope, Inc..

Clearance details

Applicant: Interscope, Inc.
Product code: Code QNE
Advisory panel: Gastroenterology, Urology
Date received: 2020-03-16
Decision date: 2020-12-23
Decision: Unknown
Clearance type: Direct
Location: Whitinsville, MA, US

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