Across
- 4. ____ device exemption
- 5. International Standards Organization
- 6. ___ Centric
- 7. ____ Evidence
- 9. Current Month
- 11. Built as ___ for my family
- 12. regulatory filing for PMA-S changes in one domain with no change to performance
Down
- 1. FDA regulates medical this element of a medical product
- 2. FDA process of scientific and regulatory review to evaluate the safety and effectiveness of Class III medical devices
- 3. 510k files produce this
- 5. Foundation of Quality
- 8. CRMs notified body
- 10. regulatory filing of a process change with no change to performance