# K943147: Statlock CV

- Pathway: 510(k) (Traditional)
- Applicant: Venetec, Inc.
- Decided: Sep 29, 1994 after 91 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
No predicates in its family tree.
7 later devices descend from it; 2 cite it directly.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K082047: Securacath Catheter, Model SPK01 (2008), 6 descendants of its own
- K083081: Modification to Securacath, Model: SPK01 (2009), 5 descendants of its own
- K092306: Securacath Universal (2010), 4 descendants of its own
- K120935: Securacath (2012), 3 descendants of its own
- K180769: SecurAcath (2018), 2 descendants of its own

Source page: https://510kreport.com/device/K943147
Methodology: https://510kreport.com/methodology