Clearance Summary
Lifetech Cardio Model 8301 Temporary Pacemaker received FDA 510(k) clearance under submission number K182839, sponsored by Shenzhen Lifetech Cardio Medical Electronics Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2019-02-28.
- Submission: K182839
- Applicant / Sponsor: Shenzhen Lifetech Cardio Medical Electronics Co., Ltd.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.3600
- Decision date: 2019-02-28
Classification & Regulation
This clearance is catalogued under FDA product code DTE and 21 CFR 870.3600, within the Cardiovascular review panel as a Class II device.