Pdmp, Inc. is one of 25313 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pdmp, Inc. - FDA 510(k) Cleared Devices
Recent clearances: NEEDLE INCAPACITATOR (NEEDLE GUARD)
1
Total
1
Cleared
0
Denied
Pdmp, Inc. has 1 FDA 510(k) cleared medical devices. Based in Crofton, US.
Historical record: 1 cleared submissions from 2004 to 2004. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Pdmp, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Entela, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Pdmp, Inc.
1 devices