Veraview X800— 510(k) K171012
Substantially EquivalentJ. Morita USA, Inc.
FDA 510(k) clearance K171012 for Veraview X800, Substantially Equivalent on 2017-12-19. Applicant: J. Morita USA, Inc.. Device class: 2.
Clearance details
- Applicant
- J. Morita USA, Inc.
- Product code
- Code OAS
- Device class
- Class 2
- Regulation
- 21 CFR 892.1750
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Irvine, CA, US
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