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. Device class: 2.
Clearance details
- Applicant
- Hitachi Medical Corp. of America
- Product code
- Code HGL
- Device class
- Class 2
- Regulation
- 21 CFR 884.2960
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Tarrytown, NY, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.