# K102418: Reverse Medical Report Guide Catheter System

- Pathway: 510(k) (Traditional)
- Applicant: Reverse Medical Corporation
- Decided: Apr 15, 2011 after 233 days
- Product code: DQY (Catheter, Percutaneous)
- Device class: 2
- Regulation: 21 CFR 870.1250
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 5 generations back to K010954 (2001). 7 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K070970: Neuron Support Catheter System, Model 5F/6F, Penumbra, Inc. (2007) Summary page 1.
- K093184: Envoy Guiding Catheters, Codman & Shurtleff, Inc. (2009) Summary page 1.
- K082385: Chaperon Guiding Catheter, MicroVention, Inc. (2008) Summary page 1.

## Most influential descendants
- K112629: Onset Access Catheter System (2011), 0 descendants of its own

## Indications for use
The Reverse Medical RePort M Guide Catheter System is indicated for the introduction of interventional/diagnostic devices into the peripheral, coronary and neuro vasculature.

Source page: https://510kreport.com/device/K102418
Methodology: https://510kreport.com/methodology