Data / Medical devices / United States / Pathpresenter Corp
Pathpresenter Corp: FDA-registered device maker in Montville, NJ, United States, 1 510(k) clearance
Pathpresenter Corp is registered with the FDA (registration 3039498387) in Montville, NJ, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated June 20, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3039498387
- Address
- 19 Louis Dr, Montville, NJ, United States, 07045
- Owner or operator
- PathPresenter (10093699)
- Roles
- Complaint file establishment, Manufacturer
- First device listed
- August 7, 2025
- Registered through
- 2026
- Brand names listed
- PathPresenter Clinical Viewer
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Digital Pathology Image Viewing And Management Software | QKQ | 2 | Complaint file establishment, Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| June 20, 2025 | K250968 | PathPresenter Clinical Viewer | QKQ | Substantially Equivalent | Pathpresenter Corporation | accessdata.fda.gov |
Compare with other makers
Updated June 20, 2025. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.