# K123194: Junctional Emergency Treatment Tool Model 30-0088

- Pathway: 510(k) (Traditional)
- Applicant: North American Rescue Products, Inc.
- Decided: Jan 3, 2013 after 84 days
- Product code: DXC (Clamp, Vascular)
- Device class: 2
- Regulation: 21 CFR 870.4450
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K002767 (2000). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K102025: Combat Ready Clamp, Combat Medical Systems, LLC (2010) Summary page 1.

## Recalls of this device
- Jul 1, 2025 · Class II · Z-2637-2025: Device used for unilateral or bilateral occlusion of blood flow to the lower limbs has a potential manufacturing defect that may compromise the structural integrity of the device and device performanc

## Indications for use
The North American Rescue Junctional Emergency Treatment Tool is indicated for emergent purposes to control difficult bleeds in the inguinal area.

Source page: https://510kreport.com/device/K123194
Methodology: https://510kreport.com/methodology