meddevicedb.com FDA Device Reference

EXALT Model B Single-Use Bronchoscope

K222014 Class II Special
Decision Date
2022-07-28
Sponsor / Applicant
Boston Scientific Corporation

Technical Specification

510(k) Submission ID K222014
Product Code EOQ
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.4680
Decision Date 2022-07-28
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EXALT Model B Single-Use Bronchoscope received FDA 510(k) clearance under submission number K222014, sponsored by Boston Scientific Corporation. The device was reviewed via the Special premarket notification pathway and assigned to the Ear, Nose, Throat review panel. The statutory decision date of record is 2022-07-28.

Classification & Regulation

This clearance is catalogued under FDA product code EOQ and 21 CFR 874.4680, within the Ear, Nose, Throat review panel as a Class II device.