# K932855: Hollister Vertical Drain/Tube Attachment Device

- Pathway: 510(k) (Traditional)
- Applicant: Hollister, Inc.
- Decided: Oct 13, 1993 after 125 days
- Product code: KNT (Tubes, Gastrointestinal (And Accessories))
- Device class: 2
- Regulation: 21 CFR 876.5980
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device 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.

## Recalls of this device
- Feb 11, 2021 · Class II · Z-1311-2021: The tube holder can separate from the barrier that secures the device to the patients' body. The tube holder has the potential failure to separate from the barrier. This separation might contribute to

Source page: https://510kreport.com/device/K932855
Methodology: https://510kreport.com/methodology