Medical Device Manufacturer · US , Irvine , CA

Artivent Corporation - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2008

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1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Artivent Corporation Anesthesiology ✕

1 devices

1-1 of 1

Cleared Sep 12, 2008

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Anesthesiology · 283d