FDA 510(k) Premarket Notification K142934: CrossCountry Transbronchial Access Tool straight, CrossCountry Transbronchial Access Tool curved

Submission Details & Decision

Normalized public record details for 510(k) notification K142934.

Source Dataset

FDA 510(k) Premarket Notifications

510(k) Number

K142934

Applicant / Sponsor

Covidien

Device Name

CrossCountry Transbronchial Access Tool straight, CrossCountry Transbronchial Access Tool curved

Product Code

EOQ

Decision Date

2015-06-17

Decision / Status

Substantially Equivalent (SESE)

Advisory Committee

Ear, Nose, Throat (EN)

Clearance Type

Traditional

Third Party Flag

Date Received

2014-10-09

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