# K152140: Boa Endoscopic Valve

- Pathway: 510(k) (Traditional)
- Applicant: C2 Therapeutics, Inc.
- Decided: Oct 13, 2015 after 71 days
- Product code: OCX (Endoscopic Irrigation/Suction System)
- Device class: 2
- Regulation: 21 CFR 876.1500
- 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 K111821 (2011). 1 ancestor in all.
1 later device descends from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K111821: Biopsy Valve, Endochoice, Inc. (2011) Summary page 4.

## Most influential descendants
- K193036: C2 CryoBalloon EndoGrip (2019), 0 descendants of its own

## Indications for use
The Boa Endoscopic Valve™ is intended to provide access for endoscopic device passage and exchange throughout the endoscopic procedure.

Source page: https://510kreport.com/device/K152140
Methodology: https://510kreport.com/methodology