Medical Device Manufacturer · GB , Kent Rainham Me8 7ed

P.K. Morgan , Ltd. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1996
4
Total
4
Cleared
0
Denied

P.K. Morgan , Ltd. has 4 FDA 510(k) cleared medical devices. Based in Kent Rainham Me8 7ed, GB.

Historical record: 4 cleared submissions from 1996 to 1997. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by P.K. Morgan , Ltd. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - P.K. Morgan , Ltd.
4 devices
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