# K072542: Maxplus Tru-Swab Positive Displacement Connector

- Pathway: 510(k) (Traditional)
- Applicant: Medegen Medical Manufacturing System
- Decided: Sep 25, 2007 after 15 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
No predicates in its family tree.
27 later devices descend from it; 1 cites it directly.
0 of 28 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K132413: MZ1000 (2013), 26 descendants of its own
- K140831: Maxzero Extension Set with Needless Connector (2014), 13 descendants of its own
- K170336: BD Nexiva Closed IV Catheter System (Single Port) with MaxZero Needleless Connector (2017), 6 descendants of its own
- K183399: BD Nexiva Closed IV Catheter System (2019), 5 descendants of its own
- K162804: Q2 Low Pressure Power Injection Extension Set (2017), 4 descendants of its own

## Indications for use
The MaxPlus is a sterile single patient use Positive Displacement Connector for needleless access to the IVline and/or IVcatheter during IVtherapy. The MaxPlus connector can be used for direct injection, intermittent infusion, continuous infusion or aspiration.

Source page: https://510kreport.com/device/K072542
Methodology: https://510kreport.com/methodology