Conavi Medical Inc.

FDA Regulatory Profile

Summary

Total Recalls
1 (1 Class I)
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent Recalls

NumberClassProductDate
Z-1585-2025Class IBrand Name: Novasight Hybrid System Product Name: Novasight Hybrid Catheter Model/Catalog Number: March 12, 2025

Recent 510(k) Clearances

K-NumberDeviceDate
K172258Novasight Hybrid SystemApril 27, 2018
K162789Foresight Intracardiac Echocardiology (ICE) SystemMarch 28, 2017