# Prodesse, Inc.

- Location (FDA's records): Waukesha, WI
- FDA decisions: 6 (2008–2009): 6 510(k) clearances
- Product codes: OCC (3), OOU (1), OEM (1), LLH (1)
- Predicates its devices cite: 8 (2 its own); citations of its devices by later devices: 36 (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
- Luminex Molecular Diagnostics, Inc.: 4 (https://510kreport.com/company/luminex-molecular-diagnostics)
- Techlab, Inc.: 1 (https://510kreport.com/company/techlab)
- Bd Diagnostics (Geneohm Sciences, Inc.): 1 (https://510kreport.com/company/bd-diagnostics-geneohm-sciences)

## Firms that cite its devices most
- Quidel Corp.: 9 (https://510kreport.com/company/quidel)
- Gen-Probe Prodesse, Inc.: 8 (https://510kreport.com/company/gen-probe-prodesse)
- Focus Diagnostics, Inc.: 6 (https://510kreport.com/company/focus-diagnostics)
- Iquum, Inc.: 3 (https://510kreport.com/company/iquum)
- Nanosphere, Inc.: 2 (https://510kreport.com/company/nanosphere)
- Hologic, Inc.: 2 (https://510kreport.com/company/hologic)
- Abbott Laboratories: 1 (https://510kreport.com/company/abbott-laboratories)
- Diagnostic Hybrids, Inc.: 1 (https://510kreport.com/company/diagnostic-hybrids)

## Its most-cited devices
- K092500: Modification to Proflu+ Assay (2009), cited by 10
- K073029: Proflu+ Assay (2008), cited by 10
- K081030: Modification to Proflu+ Assay (2008), cited by 8
- K082688: Pro HMPV+ Assay (2008), cited by 5
- K091053: Proparaflu+Assay (2009), cited by 3

## Recent decisions
- K091053: Proparaflu+Assay (Nov 20, 2009)
- K092500: Modification to Proflu+ Assay (Aug 20, 2009)
- K090239: Progastro CD Assay (Apr 16, 2009)
- K082688: Pro HMPV+ Assay (Nov 7, 2008)
- K081030: Modification to Proflu+ Assay (May 2, 2008)
- K073029: Proflu+ Assay (Jan 4, 2008)

Source page: https://510kreport.com/company/prodesse