# Norfolk Medical

- Location (FDA's records): Skokie, IL
- FDA decisions: 4 (1991–2015): 4 510(k) clearances
- Product codes: LJT (2), LJS (1), FMI (1)
- Predicates its devices cite: 11 (0 its own); citations of its devices by later devices: 1 (0 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
- Norfolk Medical Products, Inc.: 2 (https://510kreport.com/company/norfolk-medical-products)
- C.R. Bard, Inc.: 2 (https://510kreport.com/company/cr-bard)
- AngioDynamics, Inc.: 2 (https://510kreport.com/company/angiodynamics)
- Medcomp: 2 (https://510kreport.com/company/medcomp)
- Smiths Medical MD, Inc.: 1 (https://510kreport.com/company/smiths-medical-md)
- Phs Medical GmbH: 1 (https://510kreport.com/company/phs-medical)
- Arrow Intl., Inc.: 1 (https://510kreport.com/company/arrow-intl)

## Firms that cite its devices most
- Norfolk Medical Products, Inc.: 1 (https://510kreport.com/company/norfolk-medical-products)

## Its most-cited devices
- K111101: Norport CT-PC, Lucent Non-Coring Needel Infusion Set (2011), cited by 1

## Recent decisions
- K151341: Turbo High-Flow Non-coring Needle (Aug 20, 2015)
- K111101: Norport CT-PC, Lucent Non-Coring Needel Infusion Set (Aug 25, 2011)
- K911067: Norcath Vascular Access Catheters (Jun 3, 1991)
- K905646: Omegaport Subcutaneously Implanted Drug Delivery (Mar 27, 1991)

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