# K883956: Bio-Medicus Tubing Connectors

- Pathway: 510(k) (Traditional)
- Applicant: Bio Medicus, Inc.
- Decided: Oct 28, 1988 after 39 days
- Product code: DTL (Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass)
- Device class: 2
- Regulation: 21 CFR 870.4290
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
8 later devices descend from it; 1 cites it directly.
0 of 9 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
- K113845: Tubing, Conmnectors, and Accessories Wit Balance Biosurface (2012), 7 descendants of its own
- K122811: Connector Components with Balance Biosurface (2012), 5 descendants of its own
- K151523: Uncoated Tubing and Connector Components (2015), 4 descendants of its own
- K171308: Tubing Pack (2017), 3 descendants of its own
- K171979: Tubing Pack (2017), 2 descendants of its own

Source page: https://510kreport.com/device/K883956
Methodology: https://510kreport.com/methodology