Medical Device Manufacturer · US , Denton , TX

Neobit Co., Ltd. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2004
1
Total
1
Cleared
0
Denied

Neobit Co., Ltd. has 1 FDA 510(k) cleared medical devices. Based in Denton, US.

Historical record: 1 cleared submissions from 2004 to 2004. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Neobit Co., Ltd. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Neobit Co., Ltd.
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