PathPresenter Clinical Viewer— 510(k) K250968
Substantially EquivalentPathpresenter Corporation
FDA 510(k) clearance K250968 for PathPresenter Clinical Viewer, Substantially Equivalent on 2025-06-20. Applicant: Pathpresenter Corporation. Device class: 2.
Clearance details
- Applicant
- Pathpresenter Corporation
- Product code
- Code QKQ
- Device class
- Class 2
- Regulation
- 21 CFR 864.3700
- Advisory panel
- Pathology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Montville, NJ, US
Recent devices under product code QKQ
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