Medical Device Manufacturer · US , Plymouth Meeting , PA

Penrith Corporation - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2010
1
Total
1
Cleared
0
Denied

Penrith Corporation has 1 FDA 510(k) cleared medical devices. Based in Plymouth Meeting, US.

Historical record: 1 cleared submissions from 2010 to 2010. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Penrith Corporation Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Penrith Corporation
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