Medical Vision Ab
FDA Regulatory Profile
Medical Vision Ab appears in FDA public data with 1 recall, 1 510(k) clearance, 1 FDA inspection, and 0 compliance actions on record. Its most recent recall (Z-2705-2016, Class II) was initiated on May 10, 2016. Its most recent 510(k) clearance was granted on February 24, 2010.
Summary
- Total Recalls
- 1
- 510(k) Clearances
- 1
- Inspections
- 1
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|
| Z-2705-2016 | Class II | Double Pump RF Patient Cassette; Product Number: 72204055. Intended to provide fluid distension a | May 10, 2016 |
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K093409 | POWERPUMP ARTHROSCOPY SYSTEM | February 24, 2010 |