EUB-305 DIAGNOSTIC ULTRASOUND DEVICE— 510(k) K870878
Substantially EquivalentHitachi Medical Corp. of America
FDA 510(k) clearance K870878 for EUB-305 DIAGNOSTIC ULTRASOUND DEVICE, Substantially Equivalent on 1988-04-22. Applicant: Hitachi Medical Corp. of America.
Clearance details
- Applicant
- Hitachi Medical Corp. of America
- Product code
- Code DXK
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Tarrytown, NY, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.