Shenzhen Jamr Technology Co., Ltd. FDA Approvals

0 new drug approvals and 6 device clearances on file. This applicant is not matched to a listed company.

Newest first

A new drug approval is an original application; a 510(k) is a device shown equivalent to one already sold.

Product	What it is	Route	Decided
Blood Pressure Monitor (W06LT)510(k)May 20, 2026Cardiovascular	Cardiovascular	510(k)Substantially Equivalent (Traditional)	May 20, 2026
Blood Pressure Monitor (B73, BE23T)510(k)Oct 27, 2025Cardiovascular	Cardiovascular	510(k)Substantially Equivalent (Traditional)	Oct 27, 2025
Ultrasonic Fetal Doppler510(k)Jun 28, 2024Obstetrics/Gynecology	Obstetrics/Gynecology	510(k)Substantially Equivalent (Traditional)	Jun 28, 2024
Blood Pressure Monitor510(k)Mar 19, 2024Cardiovascular	Cardiovascular	510(k)Substantially Equivalent (Traditional)	Mar 19, 2024
Wrist Type Blood Pressure Monitor (W05,W1101L)510(k)Aug 25, 2023Cardiovascular	Cardiovascular	510(k)Substantially Equivalent (Traditional)	Aug 25, 2023
Upper Arm Type Blood Pressure Monitor510(k)Jul 27, 2022Cardiovascular	Cardiovascular	510(k)Substantially Equivalent (Traditional)	Jul 27, 2022