# K152625: MMS Guide Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Micro Medical Solutions, Inc.
- Decided: Mar 9, 2016 after 176 days
- Product code: KRA (Catheter, Continuous Flush)
- Device class: 2
- Regulation: 21 CFR 870.1210
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K111490 (2011). 1 ancestor in all.
2 later devices descend from it; 1 cites it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K111490: Marksman Catheter, *Refers to Different Catheter Working Lenghts, Distal Single Coiled Lengths and Distal Shaft Lengths, Ev3, Inc. (2011) Summary page 5.

## Most influential descendants
- K163231: Chameleon PTA Balloon Catheter (2017), 1 descendant of its own
- K170635: Chameleon PTA Balloon Catheter (2017), 0 descendants of its own

## Indications for use
The MMS Guide Catheter is intended for the introduction of interventional devices and infusion of diagnostic or therapeutic agents into the peripheral vasculature.

Source page: https://510kreport.com/device/K152625
Methodology: https://510kreport.com/methodology