Medical Device Manufacturer · US , Mchenry , IL

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

2 submissions · 2 cleared · Since 1983

Total

Cleared

Denied

P.K. Morgan Instruments, Inc. has 2 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 2 cleared submissions from 1983 to 1983. Primary specialty: Obstetrics & Gynecology.

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

FDA 510(k) Regulatory Record - P.K. Morgan Instruments, Inc.

2 devices

1-2 of 2