EUP-V12 5.0 MHZ CONVEX ARRAY TRANSVAGINAL PROBE— 510(k) K900966
Substantially EquivalentHitachi Medical Corp. of America
FDA 510(k) clearance K900966 for EUP-V12 5.0 MHZ CONVEX ARRAY TRANSVAGINAL PROBE, Substantially Equivalent on 1990-09-12. Applicant: Hitachi Medical Corp. of America.
Clearance details
- Applicant
- Hitachi Medical Corp. of America
- Product code
- Code HGL
- Advisory panel
- Obstetrics/Gynecology
- 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.