Penrith Corporation is one of 24595 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Penrith Corporation - FDA 510(k) Cleared Devices
Recent clearances: PENRITH ELETTRA ULTRASOUND SYSTEM
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.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Penrith Corporation
1 devices