Norfolk Medical Products, Inc.
FDA 510(k) medical device clearances.
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.