FDA 510(k) Applications Submitted by Shenzhen Lifetech Cardio Medical Electronics Co., Ltd.

FDA 510(k) Number Submission Date Device Name Applicant
K182839 10/09/2018 Lifetech Cardio Model 8301 Temporary Pacemaker Shenzhen Lifetech Cardio Medical Electronics Co., Ltd.


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact