# K994196: Horizon Medical Products Microport 2 Peripheral Access Port System

- Pathway: 510(k) (Traditional)
- Applicant: Horizon Medical Products, Inc.
- Decided: Feb 10, 2000 after 59 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
No predicates in its family tree.
8 later devices descend from it; 1 cites it directly.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Sims Deltec P.A.S. Port, Peripheral Access System: named in the summary without a submission number
- (no number) Bard Access Systems BardPort Slim Titanium Low Profile Implanted Port: named in the summary without a submission number
- (no number) Medi-Tech R-Port Premier Implantable Vascular Access System: named in the summary without a submission number

## Most influential descendants
- K032754: Vortex MP (2003), 7 descendants of its own
- K033473: Modification to Vortex MP Vascular Access Port (2003), 6 descendants of its own
- K072375: Smartport CT MP Port Access System and Lifeguard CT Safety Infusion Set (2007), 5 descendants of its own
- 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

## Indications for use
The MicroPort 2 System is indicated for peripheral placement in the midarm, above the anticubital space and well below the subaxillary area, when patient therapy requires repeated venous access for injection or infusion therapy and/or venous blood sampling.

Source page: https://510kreport.com/device/K994196
Methodology: https://510kreport.com/methodology