cmAngio® V1.0— 510(k) K232367
Substantially EquivalentCuremetrix, Inc.
FDA 510(k) clearance K232367 for cmAngio® V1.0, Substantially Equivalent on 2023-10-05. Applicant: Curemetrix, Inc..
Clearance details
- Applicant
- Curemetrix, Inc.
- Product code
- Code QIH
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- San Diego, CA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.