510(k) K232816

Device
Electrocardiograph, model: ECG301
Applicant
Shenzhen LE Medical Technology Co., Ltd.
510(k) number
K232816
Product code
DPS
Decision
Substantially Equivalent (SESE)
Decision date
2024-06-07
Date received
2023-09-13
Regulation
870.2340
Classification name
Electrocardiograph
Medical specialty
Cardiovascular
Review panel
Cardiovascular
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Related Records

Applicant Contact

Contact
Wuyaxiong .
Address
5f, Block A, Xinyongfeng Industrial Park, #2 Tianbao Rd., Yinrenshi Community, Shiyansub Shenzhen CN 518108 518108

FDA Registration Numbers

Source Documents

510(k) summary PDF

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