CorVista® System— 510(k) K232686
Substantially EquivalentCorvista Health, Inc.
FDA 510(k) clearance K232686 for CorVista® System, Substantially Equivalent on 2023-09-08. Applicant: Corvista Health, Inc.. Device class: 2.
Clearance details
- Applicant
- Corvista Health, Inc.
- Product code
- Code QXX
- Device class
- Class 2
- Regulation
- 21 CFR 870.2380
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Washington, DC, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.