# K210230: Phenom Catheters

- Pathway: 510(k) (Special)
- Applicant: Micro Therapeutics Lnc. D/B/A Ev3 Neurovascular
- Decided: Feb 25, 2021 after 28 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: 6 generations back to K945904 (1995). 12 ancestors in all.
2 later devices descend from it; 2 cite it directly.
0 of 15 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K151638: Phenom 17 Catheter, Phenom 21 Catheter, Phenom 27 Catheter, Phenom Plus Catheter, Cathera, Inc. (2015) Summary page 4.
- K180959: Phenom 27 Catheter, Cathera, Inc. (2018) Summary page 4.

## Most influential descendants
- K260199: SLIM Microcatheter (2026), 0 descendants of its own
- K251668: SurfRider 13 Microcatheter (2026), 0 descendants of its own

## Indications for use
Phenom™ Catheters are intended for the introduction of interventional devices or diagnostic agents into the neuro, peripheral, and coronary vasculatures.

Source page: https://510kreport.com/device/K210230
Methodology: https://510kreport.com/methodology