MODIFIED RADIUS - MODEL NUMBER MM 5000— 510(k) K871727
Substantially EquivalentUltrasonix, Inc.
FDA 510(k) clearance K871727 for MODIFIED RADIUS - MODEL NUMBER MM 5000, Substantially Equivalent on 1987-09-30. Applicant: Ultrasonix, Inc..
Clearance details
- Applicant
- Ultrasonix, Inc.
- Product code
- Code JOP
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- N. Yonkers, NY, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.