# K120935: Securacath

- Pathway: 510(k) (Special)
- Applicant: Interrad Medical, Inc.
- Decided: Apr 27, 2012 after 30 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: 10 generations back to K001901 (2000). 18 ancestors in all.
3 later devices descend 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)
- K092306: Securacath Universal, Interrad Medical, Inc. (2010) Summary page 2.

## Most influential descendants
- K180769: SecurAcath (2018), 2 descendants of its own
- K180994: SecurAcath 10F, SecurAcath 12F, SecurAcath 5F, SecurAcath 5F, SecurAcath 6F, SecurAcath 7F/SecurAcath 8F (2019), 1 descendant of its own
- K210629: SecurAcath (2021), 0 descendants of its own

## Indications for use
The SecurAcath Device is indicated for short or long term securement of percutaneous indwelling catheters for intravenous use to the access site by means of a subcutaneous anchor.

Source page: https://510kreport.com/device/K120935
Methodology: https://510kreport.com/methodology