Ceevra Reveal 3+— 510(k) K233568
Substantially EquivalentCeevra, Inc.
FDA 510(k) clearance K233568 for Ceevra Reveal 3+, Substantially Equivalent on 2023-12-05. Applicant: Ceevra, Inc.. Device class: 2.
Clearance details
- Applicant
- Ceevra, Inc.
- Product code
- Code QIH
- Device class
- Class 2
- Regulation
- 21 CFR 892.2050
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- San Francisco, CA, US
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