# K150280: PulmoVia Working Channel

- Pathway: 510(k) (Traditional)
- Applicant: Sanovas, Inc.
- Decided: Jun 11, 2015 after 126 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: 3 generations back to K931154 (1993). 6 ancestors in all.
No later device cites it as a predicate yet.
1 of 7 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K131234: Lungpoint Tools (Lungpoint Sheath, Lungpoint Dilation Balloon), Broncus Medical, Inc. (2013) Summary page 4.
- K112562: Bal Cath Bronchial Aspirate Sampling Catheter, Kimberly-Clark (2011) Summary page 4.

## Indications for use
The PulmoVia Working Channel is intended to be used as an access channel through which a bronchoscope and other endoscopic tools may be introduced to treat targeted tissue of the airways. The PulmoVia Working Channel can also provide means for bronchoalveolar lavage. The PulmoVia Working Channel is indicated for adult patients.

Source page: https://510kreport.com/device/K150280
Methodology: https://510kreport.com/methodology