# K180994: SecurAcath 10F, SecurAcath 12F, SecurAcath 5F, SecurAcath 5F, SecurAcath 6F, SecurAcath 7F/SecurAcath 8F

- Pathway: 510(k) (Traditional)
- Applicant: Interrad Medical, Inc.
- Decided: Jul 9, 2019 after 449 days
- Product code: KMK (Device, Intravascular Catheter Securement)
- Device class: 1
- Regulation: 21 CFR 880.5210
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 12 generations back to K001901 (2000). 20 ancestors in all.
1 later device descends from it; 1 cites it directly.
1 of 22 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K180769: SecurAcath, Interrad Medical, Inc. (2018). Cleared while this submission was under review Summary page 5.

## Most influential descendants
- K210629: SecurAcath (2021), 0 descendants of its own

## Indications for use
The SecurAcath device is indicated for catheter securement to the access site by means of subcutaneous anchors in: a) Short or long-term securement of percutaneous indwelling catheters for intravenous use b) Short or long-term securement of percutaneous indwelling catheters for abscess/general drainage

Source page: https://510kreport.com/device/K180994
Methodology: https://510kreport.com/methodology