aprevo® Digital Segmentation— 510(k) K231955
Substantially EquivalentCarlsmed, Inc.
FDA 510(k) clearance K231955 for aprevo® Digital Segmentation, Substantially Equivalent on 2023-11-03. Applicant: Carlsmed, Inc.. Device class: 2.
Clearance details
- Applicant
- Carlsmed, 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
- Traditional
- Location
- Carlsbad, CA, US
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