Veolity— 510(k) K201501
Substantially EquivalentMeVis Medical Solutions AG
FDA 510(k) clearance K201501 for Veolity, Substantially Equivalent on 2021-02-23. Applicant: MeVis Medical Solutions AG. Device class: 2.
Clearance details
- Applicant
- MeVis Medical Solutions AG
- Product code
- Code OEB
- Device class
- Class 2
- Regulation
- 21 CFR 892.2050
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Bremen, DE
Recent devices under product code OEB
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