# K911448: Multiple Biopsy Device-MBX

- Pathway: 510(k) (Traditional)
- Applicant: Triton Technology, Inc.
- Decided: Apr 16, 1991 after 32 days
- Product code: FCK (Instrument, Biopsy, Suction)
- Device class: 2
- Regulation: 21 CFR 876.1075
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 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
- K012074: XBO1-824-18/19/20 Biopsy Forceps (2001), 0 descendants of its own

Source page: https://510kreport.com/device/K911448
Methodology: https://510kreport.com/methodology