# K072375: Smartport CT MP Port Access System and Lifeguard CT Safety Infusion Set

- Pathway: 510(k) (Traditional)
- Applicant: AngioDynamics, Inc.
- Decided: Dec 13, 2007 after 112 days
- Product code: FPA (Set, Administration, Intravascular)
- Device class: 2
- Regulation: 21 CFR 880.5440
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 8 generations back to K001901 (2000). 27 ancestors in all.
5 later devices descend from it; 2 cite it directly.
0 of 33 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K060812: Powerport (TM)Implanted Titanium Port W/8 FR. Chronoflex Catheter-Multiple, C.R. Bard, Inc. (2006) Summary page 2.
- K062414: Vortex CT Port Access System and Lifeguard Safety Infusion Set, Rita Medical Systems, Inc. (2007) Summary page 2.
- K033473: Modification to Vortex MP Vascular Access Port, Horizon Medical Products, Inc. (2003) Summary page 2.
- K032754: Vortex MP, Horizon Medical Products, Inc. (2003) Summary page 2.

## Most influential descendants
- K081472: Smartport CT Vortex; LP Titanium, Single Plastic, Single Titanium, Triumph Low Profile Titanium Ports (2008), 4 descendants of its own
- K102385: Norfolk Medical Norport Family of Ports (2011), 3 descendants of its own
- K111101: Norport CT-PC, Lucent Non-Coring Needel Infusion Set (2011), 2 descendants of its own
- K112713: Norfolk Medical-Sportport-Family of Ports (2011), 1 descendant of its own
- K192291: TidalPort-AP Implantable Apheresis Vascular Access Port (2020), 0 descendants of its own

## Indications for use
The LifeGuard® CT Safety Infusion Set is indicated for use in the access of implanted vascular ports for the administration of fluids and drugs, as well as blood sampling. The 20ga and 19ga LifeGuard® CT Safety Infusion Sets are also indicated for power injection of contrast media when used with Smartport CT power injectable port access systems.

Source page: https://510kreport.com/device/K072375
Methodology: https://510kreport.com/methodology