# K003880: Concentroc HD Guide Catheter, Models 90017 (4F), 90019 (5F), 90021 (6F), 90022 (7F), 90023 (8F), 90024 (9F)

- Pathway: 510(k) (Abbreviated)
- Applicant: Concentric Medical, Inc.
- Decided: May 16, 2001 after 152 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
No predicates in its family tree.
39 later devices descend from it; 1 cites it directly.
0 of 40 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K080583: Modified HD Guide Catheter (2008), 38 descendants of its own
- K090335: HD Guide Catheter (2009), 36 descendants of its own
- K110483: Modified HD Guide Catheter (2011), 32 descendants of its own
- K133177: Modified HD Guide Catheter (2014), 28 descendants of its own
- K151667: AXS Catalyst Distal Access Catheter 058x115cm, AXS Catalyst Distal Access Catheter 058x132cm, AXS Catalyst Distal Access Catheter 060x132cm (2015), 26 descendants of its own

Source page: https://510kreport.com/device/K003880
Methodology: https://510kreport.com/methodology