# Synaptic Medical Corporation

- Location (FDA's records): Carlsbad, CA
- FDA decisions: 7 (2014–2024): 7 510(k) clearances
- Names in FDA's records: Synaptic Medical Corporation (4); Synaptic Medical Limited (3)
- Product codes: DRF (3), DRC (2), DYB (2)
- Predicates its devices cite: 6 (1 its own); citations of its devices by later devices: 1 (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 whose devices it cites most
- St Jude Medical: 3 (https://510kreport.com/company/st-jude-medical)
- Access Point Technologies Ep, Inc.: 1 (https://510kreport.com/company/access-point-technologies-ep)
- Medtronic, Inc.: 1 (https://510kreport.com/company/medtronic)

## Its most-cited devices
- K151936: Steerable Intracardiac Catheter Introducer Kit and Transseptal Needle (2015), cited by 1

## Recent decisions
- K233900: Nordica PV Cryo Mapping Catheter (Sep 6, 2024)
- K240246: Accusafe Transseptal Guidewire (GTR31180, GTR31230) (Jul 26, 2024)
- K233708: NaviGo 12F Steerable Intracardiac Catheter Introducer Kit (S12FS-01) (Feb 16, 2024)
- K203793: RithmID-SD Steerable Diagnostic Electrophysiology Catheter (Feb 14, 2022)
- K151936: Steerable Intracardiac Catheter Introducer Kit and Transseptal Needle (Dec 4, 2015)
- K132943: Intracardic Catheter Introducer Kit and Transseptal Needle (Aug 29, 2014)
- K133028: Rithm ID Electrophysiology Catheter (Mar 4, 2014)

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