# K111488: Mantaray Guidewire Model M-6000, M-6001, M-6002, M-6003

- Pathway: 510(k) (Special)
- Applicant: Bridgepoint Medical
- Decided: Jun 30, 2011 after 30 days
- Product code: DQX (Wire, Guide, Catheter)
- Device class: 2
- Regulation: 21 CFR 870.1330
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
7 later devices descend from it; 2 cite it directly.
0 of 8 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
- K120533: Bigboss Catheters Mantatay Catheter Mantaray Guidewires (2012), 5 descendants of its own
- K193596: Wingman 14, Wingman 14C, Wingman 18, Wingman 35 (2020), 1 descendant of its own
- K120881: Mantaray Guidewires (2012), 1 descendant of its own
- K262013: Kiba CTO Crossing Catheter (2026), 0 descendants of its own
- K221163: Tunnel Crossing Catheter (2023), 0 descendants of its own

Source page: https://510kreport.com/device/K111488
Methodology: https://510kreport.com/methodology