meddevicedb.com FDA Device Reference

Captura Disposable Bronchoscope Biopsy Forceps

K163377 Class II Traditional
Decision Date
2018-02-21
Sponsor / Applicant
Wilson-Cook Medical, Inc.

Technical Specification

510(k) Submission ID K163377
Product Code EOQ
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.4680
Decision Date 2018-02-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Captura Disposable Bronchoscope Biopsy Forceps received FDA 510(k) clearance under submission number K163377, sponsored by Wilson-Cook Medical, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ear, Nose, Throat review panel. The statutory decision date of record is 2018-02-21.

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.