# K012073: Olympus Spray Catheter PW-6C-1

- Pathway: 510(k) (Traditional)
- Applicant: The Olympus Optical Co.
- Decided: Aug 10, 2001 after 39 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
This instrument has been designed to be used with an Olympus endoscope for washing, and spraying contrast media or medicine (e.g. anesthetics) within the airway, including the tracheobronchial tree,

Source page: https://510kreport.com/device/K012073
Methodology: https://510kreport.com/methodology