Shanghai Microport EP Medtech Co., Ltd.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K210313EasyFinder Fixed Curve Diagnostic Catheter, Forlnk Cable for Mapping CatheterDecember 30, 2022
K212625PathBuilder Transseptal NeedleMarch 23, 2022
K212626PathBuilder Transseptal Guiding IntroducerMarch 23, 2022
K211530PathBuilder Steerable IntroducerFebruary 8, 2022