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Shenzhen Lifetech Cardio Medical Electronics Co., Ltd.

FDA Regulatory Profile

Shenzhen Lifetech Cardio Medical Electronics Co., Ltd. appears in FDA public data with 0 recalls, 2 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on January 7, 2024.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K232721Lifetech Cardio Temporary PacemakerJanuary 7, 2024
K182839Lifetech Cardio Model 8301 Temporary PacemakerFebruary 28, 2019

FDA data resources