# K171483: ArchFlo CT Midline

- Pathway: 510(k) (Traditional)
- Applicant: Medcomp (Dba Medical Components, Inc.)
- Decided: Dec 15, 2017 after 207 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 Arch-Flo CT Midline is indicated for Short-Term peripheral access to the peripheral venous system for selected intravenous therapies, blood sampling, and power injection of contrast media. This catheter may be inserted via basilic, cephalic, or median cubital vein.

Source page: https://510kreport.com/device/K171483
Methodology: https://510kreport.com/methodology