Roche Digital Pathology Dx (VENTANA DP 200)— 510(k) K232879
Substantially EquivalentVentana Medical Systems, Inc.
FDA 510(k) clearance K232879 for Roche Digital Pathology Dx (VENTANA DP 200), Substantially Equivalent on 2024-06-14. Applicant: Ventana Medical Systems, Inc.. Device class: 2.
Clearance details
- Applicant
- Ventana Medical Systems, Inc.
- Product code
- Code PSY
- Device class
- Class 2
- Regulation
- 21 CFR 864.3700
- Advisory panel
- Pathology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Tucson, AZ, US
Recent devices under product code PSY
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