# K885216: Attachable Lanz (Tentative)

- Pathway: 510(k) (Traditional)
- Applicant: Mallinckroot, Inc.
- Decided: Mar 14, 1989 after 85 days
- Product code: BSK (Cuff, Tracheal Tube, Inflatable)
- Device class: 2
- Regulation: 21 CFR 868.5750
- 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
- K112915: Spirtius Cuff Inflation Syringe (2012), 0 descendants of its own
- K110631: Venner Tracheal Seal Monitor (2011), 0 descendants of its own

Source page: https://510kreport.com/device/K885216
Methodology: https://510kreport.com/methodology