Medical Device Manufacturer · IL , Tzur Yigal

Bioprotect, Ltd. - FDA 510(k) Cleared Devices

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

Bioprotect, Ltd. has 1 FDA 510(k) cleared medical devices. Based in Tzur Yigal, IL.

Last cleared in 2023. Active since 2023. Primary specialty: Radiology.

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

510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.

FDA 510(k) Regulatory Record - Bioprotect, Ltd.
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