Lifetech Cardio Temporary Pacemaker
K-Number: K232721 · 2024-01-07
Decision Date2024-01-07
Product CodeDTE
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
Lifetech Cardio Temporary Pacemaker is a medical device manufactured by Shenzhen Lifetech Cardio Medical Electronics Co., Ltd.. It received FDA 510(k) clearance on 2024-01-07 under approval number K232721. The device is classified under product code DTE. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Lifetech Cardio Temporary Pacemaker?
Lifetech Cardio Temporary Pacemaker is a medical device that received FDA 510(k) clearance on 2024-01-07. It is manufactured by Shenzhen Lifetech Cardio Medical Electronics Co., Ltd.. The 510(k) number is K232721.
When was Lifetech Cardio Temporary Pacemaker approved by the FDA?
Lifetech Cardio Temporary Pacemaker received FDA 510(k) clearance on 2024-01-07, under approval number K232721.
What company makes Lifetech Cardio Temporary Pacemaker?
Lifetech Cardio Temporary Pacemaker is manufactured by Shenzhen Lifetech Cardio Medical Electronics Co., Ltd..
What is the FDA product code for Lifetech Cardio Temporary Pacemaker?
The FDA product code for Lifetech Cardio Temporary Pacemaker is DTE.
Other Devices by Shenzhen Lifetech Cardio Medical Electronics Co., Ltd.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.