# K894857: Pedi-Tube (R) Stylet

- Pathway: 510(k) (Traditional)
- Applicant: Biosearch Medical Products, Inc.
- Decided: Oct 3, 1989 after 64 days
- Product code: KNT (Tubes, Gastrointestinal (And Accessories))
- Device class: 2
- Regulation: 21 CFR 876.5980
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
3 later devices descend from it; 2 cite it directly.
0 of 4 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
- K960632: Kangaroo Feeding Tube Placment Stylet (1996), 2 descendants of its own
- K101199: Guide Wire for Edi Catheter, 8FR,125CM,5 Each,Guide Wire for Edi Catheter, 8FR,125CM,5 Each,Guide Wire for Edi Catheter, (2010), 1 descendant of its own
- K153461: Guide wire for Edi Catheter 6 Fr, Guide wire for Edi Catheter 8 Fr, 100 cm, Guide wire for Edi Catheter 8 Fr, 125 cm (2015), 0 descendants of its own

Source page: https://510kreport.com/device/K894857
Methodology: https://510kreport.com/methodology