Medical Device Manufacturer · US , Tinton Falls , NJ

Pausch, LLC - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2008

Total

Cleared

Denied

Pausch, LLC has 1 FDA 510(k) cleared medical devices. Based in Tinton Falls, US.

Historical record: 1 cleared submissions from 2008 to 2008. Primary specialty: Radiology.

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

FDA 510(k) Regulatory Record - Pausch, LLC

1 devices

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