# Source-Ray, Inc.

- Location (FDA's records): Bohemia, NY
- FDA decisions: 8 (2003–2016): 8 510(k) clearances
- Product codes: IZL (6), KPR (2)
- Predicates its devices cite: 1 (1 its own); citations of its devices by later devices: 2 (1 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
- Portavision Medical, LLC: 1 (https://510kreport.com/company/portavision-medical)

## Its most-cited devices
- K090655: Portable X-Ray System, Model Powermax 1260 (2009), cited by 1
- K043062: Model SR-130-D Portable Digital X-Ray System (2004), cited by 1

## Recent decisions
- K163063: UC-5000 Mobile X-Ray (Dec 12, 2016)
- K133959: Podiatry X-Ray System (Jan 22, 2015)
- K090655: Portable X-Ray System, Model Powermax 1260 (Jul 14, 2009)
- K071392: PXS-810, Podiatry X-Ray System (Aug 3, 2007)
- K062472: Optional Remote Control, Model RC-115, for Portable X-Ray System, Model SR-115 (Oct 31, 2006)
- K052001: Model SR-115 Portable X-Ray System (Aug 11, 2005)
- K043062: Model SR-130-D Portable Digital X-Ray System (Dec 13, 2004)
- K030494: SR-130 (May 20, 2003)

Source page: https://510kreport.com/company/source-ray