Shenzhen Jamr Technology Co., Ltd.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K251331Blood Pressure Monitor (B73, BE23T)October 27, 2025
K233823Ultrasonic Fetal DopplerJune 28, 2024
K233146Blood Pressure MonitorMarch 19, 2024
K230409Wrist Type Blood Pressure Monitor (W05,W1101L)August 25, 2023
K220886Upper Arm Type Blood Pressure MonitorJuly 27, 2022
K200437Blood Pressure MonitorJune 25, 2020