Synaptic Medical Corporation

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K233900Nordica PV Cryo Mapping CatheterSeptember 6, 2024
K240246Accusafe Transseptal Guidewire (GTR31180, GTR31230)July 26, 2024
K233708NaviGo 12F Steerable Intracardiac Catheter Introducer Kit (S12FS-01)February 16, 2024
K203793RithmID-SD Steerable Diagnostic Electrophysiology CatheterFebruary 14, 2022