# K140726: Captivator Emr Device for Standard Gastroscopes - Box 1, Captivator Emr Device for Standard Gastroscopes - Box 5, Captiv

- Pathway: 510(k) (Traditional)
- Applicant: Boston Scientific Corp
- Decided: Jul 21, 2014 after 119 days
- Product code: FDI (Snare, Flexible)
- Device class: 2
- Regulation: 21 CFR 876.4300
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 4 generations back to K853585 (1986). 5 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K050578: Cook Ireland Duette Multi-Band Mucosectomy Device, Cook Ireland, Ltd. (2005) Summary page 1.

## Most influential descendants
- K190512: SmartBand EMR Kit, SmartBand EMR Pack, SmartSnare (2019), 1 descendant of its own
- K212860: SmartBand EMR Kit (SB-EMR-K, SB-EMR-K-12, SB-EMR-K-9.4), SmartBand EMR Pack (SB-EMR-P, SB-EMR-P-12, SB-EMR-P-9.4), SmartSnare EMR Hexagonal Snare (SS-230-1 or packaged with kit) (2021), 0 descendants of its own

## Indications for use
The Captivatorm EMR Device is indicated for endoscopic mucosal resection in the upper GI tract.

Source page: https://510kreport.com/device/K140726
Methodology: https://510kreport.com/methodology