ANGIOVISION 1000— 510(k) K953973
Substantially EquivalentMedivision Medical Imaging, Ltd.
FDA 510(k) clearance K953973 for ANGIOVISION 1000, Substantially Equivalent on 1995-11-17. Applicant: Medivision Medical Imaging, Ltd..
Clearance details
- Applicant
- Medivision Medical Imaging, Ltd.
- Product code
- Code HKI
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Hopkinton, MA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.