# K962380: Olympus BF Type 200 Video Bronchscopes (BF-200/BF-P200/BF-IT200)

- Pathway: 510(k) (Traditional)
- Applicant: Olympus America, Inc.
- Decided: Aug 9, 1996 after 50 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
Longest line of descent: 1 generation back to K931154 (1993). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K931154: Evis 200 System, Olympus Corp. (1993) Summary page 1.

## Indications for use
The Olympus EVIS BF Type 200 Series video bronchoscopes have been designed for endoscopic diagnosis and treatment within the airways, including the tracheobronchial tree.

Source page: https://510kreport.com/device/K962380
Methodology: https://510kreport.com/methodology