# K911632: Capiox (R) Bubble Trap

- Pathway: 510(k) (Traditional)
- Applicant: Terumo Medical Corp.
- Decided: Jul 9, 1991 after 89 days
- Product code: KRL (Detector, Bubble, Cardiopulmonary Bypass)
- Device class: 2
- Regulation: 21 CFR 870.4205
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 2 cite it directly.
0 of 3 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
- K090698: Capiox Bubble Trap with X-Coating (2009), 0 descendants of its own
- K082412: Venous Bubble Trap, Model VBT 160; Venous Bubble Trap with Bioline Coating, Model BE-VBT 160, Beq-VBT 160 (2008), 0 descendants of its own

Source page: https://510kreport.com/device/K911632
Methodology: https://510kreport.com/methodology