EndoRotor Device— 510(k) DEN200016
UnknownInterscope, Inc.
FDA 510(k) clearance DEN200016 for EndoRotor Device, Unknown on 2020-12-23. Applicant: Interscope, Inc.. Device class: 2.
Clearance details
- Applicant
- Interscope, Inc.
- Product code
- Code QNE
- Device class
- Class 2
- Regulation
- 21 CFR 876.4330
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Direct
- Location
- Whitinsville, MA, US
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