# K214048: Millipede 088 Access Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Perfuze, Ltd.
- Decided: Sep 20, 2022 after 267 days
- Product code: QJP (Catheter, Percutaneous, Neurovasculature)
- 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: 8 generations back to K010954 (2001). 13 ancestors in all.
6 later devices descend from it; 1 cites it directly.
0 of 20 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K203764: TracStar Large Distal Platform, ZOOM 88 Large Distal Platform, ZOOM 88-T Large Distal Platform, Imperative Care, Inc. (2021) Summary page 4.

## Most influential descendants
- K231802: Millipede 088 Access Catheter (2023), 5 descendants of its own
- K233648: Millipede 088 Access Catheter (2023), 4 descendants of its own
- K242504: Millipede 088 Access Catheter; Millipede 070 Aspiration Catheter; Perfuze Aspiration Tube Set (2024), 3 descendants of its own
- K250012: Millipede 070 Aspiration Catheter; Perfuze Aspiration Tube Set (2025), 1 descendant of its own
- K253901: Millipede88 Access Catheter (2026), 0 descendants of its own

## Indications for use
The Millipede 088 Access Catheter is indicated for use in facilitating the insertion and guidance of microcatheters into a selected blood vessel in the neurovasculature.

Source page: https://510kreport.com/device/K214048
Methodology: https://510kreport.com/methodology
