# Portavision Medical, LLC

- Location (FDA's records): Jefferson, LA
- FDA decisions: 6 (2007–2021): 6 510(k) clearances
- Names in FDA's records: Portavision Medical, LLC (5); Portavision Medical (1)
- Product codes: OWB (3), MQB (1), IZL (1), IXK (1)
- 510(k) review time since 2016: median 64 days, against 60 for FDA's reviews in the same codes and years (2 of 3 faster)
- Predicates its devices cite: 7 (2 its own); citations of its devices by later devices: 6 (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
- Source-Ray, Inc.: 1 (https://510kreport.com/company/source-ray)
- Dynarad Corp.: 1 (https://510kreport.com/company/dynarad)
- Ecotron Co., Ltd.: 1 (https://510kreport.com/company/ecotron)
- Varian Medical Systems, Inc.: 1 (https://510kreport.com/company/varian-medical-systems)
- Enhanced Imaging Technologies, Inc.: 1 (https://510kreport.com/company/enhanced-imaging-technologies)

## Firms that cite its devices most
- Medicatech USA: 1 (https://510kreport.com/company/medicatech-usa)
- Oxos Medical, Inc.: 1 (https://510kreport.com/company/oxos-medical)
- Imagexray, LLC: 1 (https://510kreport.com/company/imagexray)
- Imaging Engineering, LLC: 1 (https://510kreport.com/company/imaging-engineering)

## Its most-cited devices
- K211191: Virtual C DRF Digital Imaging System (2021), cited by 3
- K191503: MobileRay Pulse SE Digital Imaging System (2019), cited by 2
- K212557: Virtual C DRF-NEO Digital Imaging System (2021), cited by 1

## Recent decisions
- K212557: Virtual C DRF-NEO Digital Imaging System (Sep 24, 2021)
- K211191: Virtual C DRF Digital Imaging System (Jun 24, 2021)
- K191503: MobileRay Pulse SE Digital Imaging System (Sep 4, 2019)
- K133524: Pvmed DDR 2430T (Apr 16, 2014)
- K083048: Neoray DR 2520 Digital Imaging System (Nov 21, 2008)
- K072766: Pvmed DDR 2520 Digital Imaging System (Dec 11, 2007)

Source page: https://510kreport.com/company/portavision-medical