Medical Device Manufacturer · US , Princeton , NJ

Careox, LLC - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2022
1
Total
1
Cleared
0
Denied

Careox, LLC has 1 FDA 510(k) cleared medical devices. Based in Princeton, US.

Last cleared in 2022. Active since 2022. Primary specialty: Anesthesiology.

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

510(k) submissions have been managed by ProMedic Consulting, LLC as regulatory consultant.

FDA 510(k) Regulatory Record - Careox, LLC
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