# K252050: Disposable Biopsy Forceps FB-211D, FB-221D, FB-231D, FB-241D

- Pathway: 510(k) (Traditional)
- Applicant: Olympus Medical Systems Corporation
- Decided: Mar 20, 2026 after 262 days
- Product code: EOB (Nasopharyngoscope (Flexible Or Rigid))
- Device class: 2
- Regulation: 21 CFR 874.4760
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 4 generations back to K931154 (1993). 9 ancestors in all.
No later device cites it as a predicate yet.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K013591: Xenf-TP Rhino-Laryngofiberscope, Its Acessories and Ancillary Equipment, Olympus Optical Co., Ltd. (2001) Summary page 5.

## Indications for use
The Disposable Biopsy Forceps FB-211D/221D/231D/241D are intended to be used to collect tissue within the upper airways in combination with a rhino-laryngoscope.

Source page: https://510kreport.com/device/K252050
Methodology: https://510kreport.com/methodology