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.. Device class: 2.
Clearance details
- Applicant
- Medivision Medical Imaging, Ltd.
- Product code
- Code HKI
- Device class
- Class 2
- Regulation
- 21 CFR 886.1120
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Hopkinton, MA, US
Recent devices under product code HKI
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