# K142241: LARIAT sulture Delivery Device

- Pathway: 510(k) (Special)
- Applicant: Sentreheart, Inc.
- Decided: Sep 12, 2014 after 30 days
- Product code: GAT (Suture, Nonabsorbable, Synthetic, Polyethylene)
- Device class: 2
- Regulation: 21 CFR 878.5000
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 4 generations back to K931994 (1994). 9 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 11 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K090385: Lariat II Suture Delivery Device, Sentreheart, Inc. (2009) Summary page 4.

## Most influential descendants
- K153096: LARIAT RS Suture Delivery Device (2015), 0 descendants of its own

## Indications for use
The LARIAT® III Suture Delivery Device facilitates suture placement and knot tying for use in surgical applications where soft tissue are being approximated and/or ligated with a pre-tied polyester suture.

Source page: https://510kreport.com/device/K142241
Methodology: https://510kreport.com/methodology