Medical Device Manufacturer · US , Hershey , PA

Intravent Medical Partners, LP - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2021
1
Total
1
Cleared
0
Denied

Intravent Medical Partners, LP has 1 FDA 510(k) cleared medical devices. Based in Hershey, US.

Last cleared in 2021. Active since 2021. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by Intravent Medical Partners, LP Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Msquared Associates, Inc. as regulatory consultant.

FDA 510(k) Regulatory Record - Intravent Medical Partners, LP
1 devices
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