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..
Clearance details
- Applicant
- Carlsmed, Inc.
- Product code
- Code QIH
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Carlsbad, CA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.