# Abbott Electrophysiology

- Location (FDA's records): Menlo Park, CA
- FDA decisions: 4 (2016–2017): 4 510(k) clearances
- Product codes: MTD (2), DQK (2)
- Predicates its devices cite: 9 (2 its own); citations of its devices by later devices: 4 (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
- Topera, Inc.: 7 (https://510kreport.com/company/topera)

## Firms that cite its devices most
- Ablacon, Inc.: 2 (https://510kreport.com/company/ablacon)

## Its most-cited devices
- K153093: FIRMap Catheter (2016), cited by 1
- K163709: FIRMap Catheter (2017), cited by 1
- K161240: Rhythm View Workstation (non-streaming) (2016), cited by 1
- K171583: RhythmView Workstation (2017), cited by 1

## Recent decisions
- K171583: RhythmView Workstation (Sep 1, 2017)
- K163709: FIRMap Catheter (Feb 28, 2017)
- K161240: Rhythm View Workstation (non-streaming) (Aug 10, 2016)
- K153093: FIRMap Catheter (Apr 7, 2016)

Source page: https://510kreport.com/company/abbott-electrophysiology