# K092306: Securacath Universal

- Pathway: 510(k) (Traditional)
- Applicant: Interrad Medical, Inc.
- Decided: Jul 9, 2010 after 345 days
- Product code: LJS (Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days)
- 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: 9 generations back to K001901 (2000). 17 ancestors in all.
4 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)
- K082047: Securacath Catheter, Model SPK01, Interrad Medical, Inc. (2008) Summary page 1.
- K083081: Modification to Securacath, Model: SPK01, Interrad Medical, Inc. (2009) Summary page 1.
- K943147: Statlock CV, Venetec, Inc. (1994) Summary page 1.
- (no number) Arrow Staple Anchoring Device: named in the summary without a submission number

## Most influential descendants
- K120935: Securacath (2012), 3 descendants of its own
- 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 Universal 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/K092306
Methodology: https://510kreport.com/methodology