Norfolk Medical Products, Inc.
Norfolk Medical Products, Inc. holds FDA 510(k) medical device clearances, first cleared 1983, most recent 2020.
Top product codes for Norfolk Medical Products, Inc.
Recent clearances by Norfolk Medical Products, Inc.
- K192291 — TidalPort-AP Implantable Apheresis Vascular Access Port
- K112713 — NORFOLK MEDICAL-SPORTPORT-FAMILY OF PORTS
- K102385 — NORFOLK MEDICAL NORPORT FAMILY OF PORTS
- K942784 — NORFOLK OMEGA PORT-LP SUBCUTANEOUSLY IMPLANTED
- K896544 — MD2 PERSONAL INFUSION SYSTEM
- K872838 — NORFOLK NORPORT (TM) -SP (SKIN PARALLEL)
- K871209 — NORFOLK MEDICAL NORPORT
- K871192 — SUBCUTANEOUSLY IMPLANTED DRUG DELIVERY DEPOT
- K870187 — NORFOLK NORPORT, SUBCUT. IMPLANTED DRUG DEL. DEPOT
- K870519 — SUBCUTANEOUSLY IMPLANTED DRUG DELIVERY DEPOT
- K870188 — NORFOLK MEDICAL BUTTERFLY INFUSION SET
- K863723 — NORFOLK NORPORT/SUBCUTAN. IMPLANTED DRUG DEPOT
- K863721 — NORFOLK MEDICAL POSI-GRIP 'HUBER POINT' NEEDLE
- K854593 — NORFOLK MEDICAL PERITONEAL-ACCESS PORT
- K841679 — VASCULAR-ACCESS-PORT WITHDRAWL-BLOOD
- K840788 — VASCULAR ACCESS PORT CHANGES IN MATER
- K841149 — VASCULAR-ACCESS PORT - ENLARGEMENT
- K841150 — VASCULAR-ACCESS PORT CHANGE CATHETER
- K823845 — PORT-LOCK
- K830000 — VASCULAR-ACCESS-PORT
Data sourced from openFDA. This site is unofficial and independent of the FDA.