# Dana Products, Inc.

- Location (FDA's records): South Barrington, IL
- FDA decisions: 9 (2002–2014): 9 510(k) clearances
- Product codes: JOJ (6), FRC (3)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 4 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- STERIS Corporation: 4 (https://510kreport.com/company/steris)

## Its most-cited devices
- K012195: Steam Sterilization Intergrator (2002), cited by 3
- K133267: Dana Reusable Test Pack (2014), cited by 1

## Recent decisions
- K133267: Dana Reusable Test Pack (Feb 11, 2014)
- K130135: Dana Reusable BI Test Pack (Nov 25, 2013)
- K120592: Dana Reusable Bowie Test Pack for Dana Bowie Dick Indicators (Feb 27, 2013)
- K110253: Reusable Test Pack for Dana Emulating Indicators (Apr 29, 2011)
- K103321: Dana Reusable Testpack for Steam Sterilization for 10 Minute Extended Cycles (Feb 16, 2011)
- K100891: Dana Emulating Indicator (Jan 13, 2011)
- K102761: Dana Reusable Test Pack for Steam Sterilization (Dec 20, 2010)
- K092944: Dana Reusable Test Pack for Steam Sterilization (Mar 18, 2010)

Source page: https://510kreport.com/company/dana-products