# K122684: Reverse Medical Microcatheter

- Pathway: 510(k) (Traditional)
- Applicant: Reverse Medical Corporation
- Decided: Dec 7, 2012 after 98 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: 4 generations back to K960806 (1996). 6 ancestors in all.
2 later devices descend 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)
- K083343: Headway 17 Microcatheter, MicroVention, Inc. (2008) Summary page 2.
- K001966: Rebar Micro Catheter: Rebar-18 [2.3F], 110 CM, 130 CM, 153 CM, Single Marker Band and 153 CM, Dual Marker Band, Micro Therapeutics, Inc. (2000) Summary page 2.

## Most influential descendants
- K130858: Reverse Medical Microcatheter (2013), 1 descendant of its own
- K171268: Reverse 021 Micro Catheter, Reverse 027 Micro Catheter (2017), 0 descendants of its own

## Indications for use
The Reverse Medical Microcatheter is intended for use in neuro, peripheral and coronary vasculature for the infusion of diagnostic agents such as contrast media, and therapeutic agents such as occlusion coils.

Source page: https://510kreport.com/device/K122684
Methodology: https://510kreport.com/methodology