# K170770: CT Midline

- Pathway: 510(k) (Special)
- Applicant: Medical Components, Inc. (dba MedComp)
- Decided: Jul 25, 2017 after 133 days
- Product code: PND (Midline Catheter)
- Device class: 2
- Regulation: 21 CFR 880.5200
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 10 generations back to K001901 (2000). 27 ancestors in all.
No later device cites it as a predicate yet.
2 of 28 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K141151: CT Midline, Medcomp (Medical Components, Inc.) (2014) Summary page 4.

## 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/K170770
Methodology: https://510kreport.com/methodology