Norfolk Medical Products, Inc. - FDA 510(k) Cleared Devices
20
Total
20
Cleared
0
Denied
Norfolk Medical Products, Inc. has 20 FDA 510(k) cleared general hospital devices. Based in Walker, US.
Historical record: 20 cleared submissions from 1983 to 2020.
Browse the complete list of FDA 510(k) cleared general hospital devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Norfolk Medical Products, Inc.
20 devices
Cleared
Aug 20, 2020
TidalPort-AP Implantable Apheresis Vascular Access Port
General Hospital
363d
Cleared
Oct 27, 2011
NORFOLK MEDICAL-SPORTPORT-FAMILY OF PORTS
General Hospital
38d
Cleared
Jan 14, 2011
NORFOLK MEDICAL NORPORT FAMILY OF PORTS
General Hospital
144d
Cleared
May 02, 1995
NORFOLK OMEGA PORT-LP SUBCUTANEOUSLY IMPLANTED
General Hospital
322d
Cleared
May 02, 1990
MD2 PERSONAL INFUSION SYSTEM
General Hospital
166d
Cleared
Aug 25, 1987
NORFOLK NORPORT (TM) -SP (SKIN PARALLEL)
General Hospital
36d
Cleared
Jun 24, 1987
NORFOLK MEDICAL NORPORT
General Hospital
91d
Cleared
Jun 10, 1987
SUBCUTANEOUSLY IMPLANTED DRUG DELIVERY DEPOT
General Hospital
78d
Cleared
May 07, 1987
NORFOLK NORPORT, SUBCUT. IMPLANTED DRUG DEL. DEPOT
General Hospital
111d
Cleared
Apr 15, 1987
SUBCUTANEOUSLY IMPLANTED DRUG DELIVERY DEPOT
General Hospital
68d
Cleared
Feb 10, 1987
NORFOLK MEDICAL BUTTERFLY INFUSION SET
General Hospital
25d
Cleared
Oct 29, 1986
NORFOLK NORPORT/SUBCUTAN. IMPLANTED DRUG DEPOT
General Hospital
36d