# K231802: Millipede 088 Access Catheter

- Pathway: 510(k) (Special)
- Applicant: Perfuze, Ltd.
- Decided: Sep 19, 2023 after 91 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: 9 generations back to K010954 (2001). 14 ancestors in all.
5 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)
- K214048: Millipede 088 Access Catheter, Perfuze, Ltd. (2022) Summary page 4.

## Most influential descendants
- 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
- K252392: Millipede70 Aspiration Catheter; Perfuze Aspiration Tube Set (2025), 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/K231802
Methodology: https://510kreport.com/methodology