Norfolk Medical is one of 5024 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Norfolk Medical - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Norfolk Medical has 4 FDA 510(k) cleared medical devices. Based in Skokie, US.
Historical record: 4 cleared submissions from 1991 to 2015. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Norfolk Medical Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Norfolk Medical
4 devices
Cleared
Aug 20, 2015
Turbo High-Flow Non-coring Needle
General Hospital
93d
Cleared
Aug 25, 2011
NORPORT CT-PC, LUCENT NON-CORING NEEDEL INFUSION SET
General Hospital
127d
Cleared
Jun 03, 1991
NORCATH VASCULAR ACCESS CATHETERS
General Hospital
84d
Cleared
Mar 27, 1991
OMEGAPORT SUBCUTANEOUSLY IMPLANTED DRUG DELIVERY
General Hospital
100d