Entax Ultrasound Video Bronchoscope EB-1970UK + Hi Visin Preirus

FDA 510(k) K131946 · Pentax Medical Company

Substantially Equivalent

510(k) numberK131946

Submission

Device name
Entax Ultrasound Video Bronchoscope EB-1970UK + Hi Visin Preirus
Applicant
Pentax Medical Company
Montvale, NJ, US
Received
June 27, 2013
Decision date
April 25, 2014
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
EOQ – Bronchoscope (Flexible Or Rigid)
Device class
Class II (moderate risk)
Regulation
21 CFR 874.4680
Specialty
Ear, Nose, Throat

A bronchoscope (flexible or rigid) and accessories is a tubular endoscopic device with any of a group of accessory devices which attach to the bronchoscope and is intended to examine or treat the larynx and tracheobronchial tree. If the device is reprocessed, reprocessing validation data for this device type must be included in a 510(k) submission. If the device is reusable, validated…

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Questions and answers

When was Entax Ultrasound Video Bronchoscope EB-1970UK + Hi Visin Preirus cleared by the FDA?

Entax Ultrasound Video Bronchoscope EB-1970UK + Hi Visin Preirus (K131946) received a 510(k) decision of Substantially Equivalent on April 25, 2014, 302 days after the submission was received.

What is the product code of K131946?

The FDA product code is EOQ – Bronchoscope (Flexible Or Rigid), a Class II (moderate risk) device regulated under 21 CFR 874.4680.