# K112713: Norfolk Medical-Sportport-Family of Ports

- Pathway: 510(k) (Special)
- Applicant: Norfolk Medical Products, Inc.
- Decided: Oct 27, 2011 after 38 days
- Product code: LJT (Port & Catheter, Implanted, Subcutaneous, Intravascular)
- Device class: 2
- Regulation: 21 CFR 880.5965
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 12 generations back to K001901 (2000). 61 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 63 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K111101: Norport CT-PC, Lucent Non-Coring Needel Infusion Set, Norfolk Medical (2011)

## Most influential descendants
- K192291: TidalPort-AP Implantable Apheresis Vascular Access Port (2020), 0 descendants of its own

## Indications for use
The SportPort TM is indicated for use when the patient requires the following: repeated access to the vascular system for injections, infusion of dmugs, administration of blood or blood products, and/or withdrawal of blood as part of the therapy regimen. When used with a power injectable needle infusion set, the SportPortTM is indicated for power injection of contrast media. For power injection of contrast media, the maximum recommended infusion rate is 5 mi/s with a 19 or 20 gauge non-coring power injectable needle and 2 mI/s with a 22-gauge non-coring power injectable needle.

Source page: https://510kreport.com/device/K112713
Methodology: https://510kreport.com/methodology