Regulatory filing

fda_510k (us_fda)

FDA 510(k) clearance for MicroPort MedBot ANT-X automatic robotic device.

fda 510k · cleared · decided 2024-01-01

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Key facts

Jurisdiction: us_fda
Filing type: fda 510k
Status: cleared
Filing date: 2024-01-01
Decision date: 2024-01-01
Verification posture: verified

Applicant

MicroPort MedBot

Covered models (1)

Toumai

Sources (1)

https://microport.com/news/ndr-medical-technology-a-portfolio-company-of-microport-medbot-wins-fda-510k-clearance-for-its-ant-x-automatic-robotic-device

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Identity

cd35170e-b227-407c-97f9-1b104b59d928