SPECTRADIGITAL SERIES V250DSP— 510(k) K954129
Substantially EquivalentHitachi Medical Corp. of America
FDA 510(k) clearance K954129 for SPECTRADIGITAL SERIES V250DSP, Substantially Equivalent on 1995-12-22. Applicant: Hitachi Medical Corp. of America. Device class: 2.
Clearance details
- Applicant
- Hitachi Medical Corp. of America
- Product code
- Code KPS
- Device class
- Class 2
- Regulation
- 21 CFR 892.1200
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Macedonia, OH, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.