# K210629: SecurAcath

- Pathway: 510(k) (Special)
- Applicant: Interrad Medical, Inc.
- Decided: Apr 12, 2021 after 41 days
- Product code: OKC (Implanted Subcutaneous Securement Catheter)
- 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: 13 generations back to K001901 (2000). 21 ancestors in all.
No later device cites it as a predicate yet.
1 of 22 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K180994: SecurAcath 10F, SecurAcath 12F, SecurAcath 5F, SecurAcath 5F, SecurAcath 6F, SecurAcath 7F/SecurAcath 8F, Interrad Medical, Inc. (2019) Summary page 5.

## 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 and long-term securement of percutaneous indwelling catheter for abscess/general drainage

Source page: https://510kreport.com/device/K210629
Methodology: https://510kreport.com/methodology