# Pathwork Diagnostics, Inc.

- Location (FDA's records): Palo Alto, CA
- FDA decisions: 3 (2008–2012): 3 510(k) clearances
- Names in FDA's records: Pathwork Diagnostics, Inc. (2); Pathwork Diagnostics (1)
- Product codes: OIW (3)
- Predicates its devices cite: 3 (2 its own); citations of its devices by later devices: 3 (2 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Bio-Rad Laboratories, Inc.: 1 (https://510kreport.com/company/bio-rad-laboratories)

## Firms that cite its devices most
- Cancer Genetics, Inc.: 1 (https://510kreport.com/company/cancer-genetics)

## Its most-cited devices
- K120489: Tissue of Origin Test Kit Ffpe (2012), cited by 1
- K092967: Pathwork Tissue of Origin Test Kit-Ffpe (Origin Test Kit-Ffpe (2010), cited by 1
- K080896: Pathwork Diagnostics Tissue of Origin Test (2008), cited by 1

## Recent decisions
- K120489: Tissue of Origin Test Kit Ffpe (May 17, 2012)
- K092967: Pathwork Tissue of Origin Test Kit-Ffpe (Origin Test Kit-Ffpe (Jun 8, 2010)
- K080896: Pathwork Diagnostics Tissue of Origin Test (Jul 30, 2008)

Source page: https://510kreport.com/company/pathwork-diagnostics