# K962367: Olympus Basket Graspers

- Pathway: 510(k) (Traditional)
- Applicant: Olympus America, Inc.
- Decided: Aug 5, 1996 after 47 days
- Product code: EOQ (Bronchoscope (Flexible Or Rigid))
- Device class: 2
- Regulation: 21 CFR 874.4680
- 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; 1 cites 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
- K020765: Microvasive Zero Tip Airway Retrieval Basket, Models M00513200 and M00513210 (2002), 2 descendants of its own
- K254040: LungFlow Basket Catheter (2026), 0 descendants of its own
- K250263: Disposable Grasping Forceps FG-52D/FG-54D (2025), 0 descendants of its own

Source page: https://510kreport.com/device/K962367
Methodology: https://510kreport.com/methodology