# K000570: Blue Max Balloon Dilatation Catheter, Maxforce Balloon Catheter, XXL Balloon Dilatation Cathater, Symmetry Balloon Dila

- Pathway: 510(k) (Special)
- Applicant: Boston Scientific Corp
- Decided: Apr 13, 2000 after 51 days
- Product code: LIT (Catheter, Angioplasty, Peripheral, Transluminal)
- 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.
1 later device descends from it; 1 cites it directly.
0 of 2 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
- K071309: Blue Max Balloon Dilatation Catheter (2007), 0 descendants of its own

Source page: https://510kreport.com/device/K000570
Methodology: https://510kreport.com/methodology