Medical Device Manufacturer · CN , Xiamen

Xiamen Intretech, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2023
1
Total
1
Cleared
0
Denied

Xiamen Intretech, Inc. has 1 FDA 510(k) cleared medical devices. Based in Xiamen, CN.

Last cleared in 2023. Active since 2023. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Xiamen Intretech, Inc. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Natural Cycles as regulatory consultant.

FDA 510(k) Regulatory Record - Xiamen Intretech, Inc.
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