# Rhythmia Medical, Inc.

- Location (FDA's records): Burlington, MA
- FDA decisions: 3 (2013–2015): 3 510(k) clearances
- Product codes: DRF (2), DQK (1)
- Predicates its devices cite: 4 (1 its own); citations of its devices by later devices: 3 (1 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Biosense Webster, Inc.: 1 (https://510kreport.com/company/biosense-webster)
- St Jude Medical: 1 (https://510kreport.com/company/st-jude-medical)
- Catheffects, LLC: 1 (https://510kreport.com/company/catheffects)

## Firms that cite its devices most
- Boston Scientific Corp: 2 (https://510kreport.com/company/boston-scientific)

## Its most-cited devices
- K130750: Rhythmia Mapping System (2013), cited by 1
- K143481: IntellaMap Orion High Resolution Mapping Catheter (2015), cited by 1
- K122461: Rhythmia Mapping Catheter (2013), cited by 1

## Recent decisions
- K143481: IntellaMap Orion High Resolution Mapping Catheter (Jan 8, 2015)
- K130750: Rhythmia Mapping System (Jul 22, 2013)
- K122461: Rhythmia Mapping Catheter (Apr 18, 2013)

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