# Norfolk Medical Products, Inc.

- Location (FDA's records): Skokie, IL
- FDA decisions: 20 (1983–2020): 20 510(k) clearances
- Product codes: LJT (14), FPA (2), PTD (1), LMQ (1), FRN (1)
- Predicates its devices cite: 11 (6 its own); citations of its devices by later devices: 9 (6 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- C.R. Bard, Inc.: 2 (https://510kreport.com/company/cr-bard)
- Norfolk Medical: 1 (https://510kreport.com/company/norfolk-medical)
- Phs Medical GmbH: 1 (https://510kreport.com/company/phs-medical)
- AngioDynamics, Inc.: 1 (https://510kreport.com/company/angiodynamics)

## Firms that cite its devices most
- Norfolk Medical: 2 (https://510kreport.com/company/norfolk-medical)
- Clinisurg Vascular Products, LLC: 1 (https://510kreport.com/company/clinisurg-vascular-products)

## Its most-cited devices
- K830000: Vascular-Access-Port (1983), cited by 2
- K871209: Norfolk Medical Norport (1987), cited by 1
- K871192: Subcutaneously Implanted Drug Delivery Depot (1987), cited by 1
- K863721: Norfolk Medical Posi-Grip 'Huber Point' Needle (1986), cited by 1
- K112713: Norfolk Medical-Sportport-Family of Ports (2011), cited by 1
- K840788: Vascular Access Port Changes in Mater (1984), cited by 1

## Recent decisions
- K192291: TidalPort-AP Implantable Apheresis Vascular Access Port (Aug 20, 2020)
- K112713: Norfolk Medical-Sportport-Family of Ports (Oct 27, 2011)
- K102385: Norfolk Medical Norport Family of Ports (Jan 14, 2011)
- K942784: Norfolk Omega Port-LP Subcutaneously Implanted (May 2, 1995)
- K896544: MD2 Personal Infusion System (May 2, 1990)
- K872838: Norfolk Norport (TM) -SP (Skin Parallel) (Aug 25, 1987)
- K871209: Norfolk Medical Norport (Jun 24, 1987)
- K871192: Subcutaneously Implanted Drug Delivery Depot (Jun 10, 1987)

Source page: https://510kreport.com/company/norfolk-medical-products