# Oncology Data Systems, Inc.

- Location (FDA's records): Oklahoma City, OK
- FDA decisions: 4 (2001–2010): 4 510(k) clearances
- Product codes: IYE (3), LHN (1)
- Predicates its devices cite: 9 (4 its own); citations of its devices by later devices: 7 (4 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
- Medical Dosimetry Services, Inc.: 2 (https://510kreport.com/company/medical-dosimetry-services)
- Elekta Instrument AB: 1 (https://510kreport.com/company/elekta-instrument)
- Lifeline Software, Inc.: 1 (https://510kreport.com/company/lifeline-software)
- Nucletron Corp.: 1 (https://510kreport.com/company/nucletron)

## Firms that cite its devices most
- Scanditronix Wellhofer GmbH: 1 (https://510kreport.com/company/scanditronix-wellhofer)
- Lifeline Software, Inc.: 1 (https://510kreport.com/company/lifeline-software)
- Standard Imaging, Inc.: 1 (https://510kreport.com/company/standard-imaging)

## Its most-cited devices
- K012227: Mucheck - Monitor Unit Validation Program, Model V4.1 (2001), cited by 3
- K061152: Mucheck V7.0 (2006), cited by 3
- K091602: Mucheck V8 (2009), cited by 1

## Recent decisions
- K102583: Mucheck, Version 9.0 (Nov 2, 2010)
- K091602: Mucheck V8 (Jun 18, 2009)
- K061152: Mucheck V7.0 (May 10, 2006)
- K012227: Mucheck - Monitor Unit Validation Program, Model V4.1 (Oct 1, 2001)

Source page: https://510kreport.com/company/oncology-data-systems