MeVis Liver Suite— 510(k) K232045
Substantially EquivalentMeVis Medical Solutions AG
FDA 510(k) clearance K232045 for MeVis Liver Suite, Substantially Equivalent on 2023-10-27. Applicant: MeVis Medical Solutions AG. Device class: 2.
Clearance details
- Applicant
- MeVis Medical Solutions AG
- Product code
- Code JAK
- Device class
- Class 2
- Regulation
- 21 CFR 892.1750
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Bremen, DE
Recent devices under product code JAK
view allMore clearances from MeVis Medical Solutions AG
view allAdverse events under product code JAK
product code JAK- Death
- 27
- Injury
- 571
- Malfunction
- 779
- Total
- 1,377
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.