# K141151: CT Midline

- Pathway: 510(k) (Traditional)
- Applicant: Medcomp (Medical Components, Inc.)
- Decided: Jul 8, 2014 after 64 days
- Product code: LJS (Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days)
- Device class: 2
- Regulation: 21 CFR 880.5970
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 9 generations back to K001901 (2000). 26 ancestors in all.
8 later devices descend from it; 3 cite it directly.
2 of 35 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K121094: Medcomp Vascu-Picc & Midline Catheters, Medical Components, Inc. (2012) Summary page 1.
- K091953: Pro-Picc, Medcomp (2009) Summary page 1.

## Most influential descendants
- K153393: PowerMidline Catheter (2016), 5 descendants of its own
- K173114: primeMidline Catheters (2018), 1 descendant of its own
- K162900: PowerMidline Catheter (2016), 1 descendant of its own
- K213203: Provena (TM) Midline Catheter (2022), 0 descendants of its own
- K192802: primeMidline Catheters (2019), 0 descendants of its own

## Indications for use
The CT Midlines are indicated for Short-Term peripheral access to the peripheral venous system for selected intravenous therapies, blood sampling, and power injection of contrast media. The maximum recommended infusion rate varies by catheter French size and is printed on the catheter.

Source page: https://510kreport.com/device/K141151
Methodology: https://510kreport.com/methodology