# K993900: Coagulation Electrode, Model 2000; Radiofrequency Generator, Model 20-115

- Pathway: 510(k) (Traditional)
- Applicant: Broncus Technologies, Inc.
- Decided: Jan 28, 2000 after 73 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.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Broncus™ Bronchial Catheter System: named in the summary without a submission number
- (no number) Coagulation Electrode: named in the summary without a submission number
- (no number) Force 2 Electrosurgical Generator: named in the summary without a submission number

## Indications for use
The Broncus™ Coagulation Electrode System is intended for coagulation or hemostasis in the tracheobronchial tree.

Source page: https://510kreport.com/device/K993900
Methodology: https://510kreport.com/methodology