remOVE System— 510(k) DEN160014
UnknownOvesco Endoscopy AG
FDA 510(k) clearance DEN160014 for remOVE System, Unknown on 2017-12-22. Applicant: Ovesco Endoscopy AG. Device class: 2.
Clearance details
- Applicant
- Ovesco Endoscopy AG
- Product code
- Code QAG
- Device class
- Class 2
- Regulation
- 21 CFR 876.4310
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Direct
- Location
- Tuebingen, DE
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