Hybrid3D— 510(k) K163394
Substantially EquivalentHermes Medical Solutions AB
FDA 510(k) clearance K163394 for Hybrid3D, Substantially Equivalent on 2017-05-22. Applicant: Hermes Medical Solutions AB.
Clearance details
- Applicant
- Hermes Medical Solutions AB
- Product code
- Code KPS
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Stockholm, SE
Data sourced from openFDA. This site is unofficial and independent of the FDA.