FDA 510(k)

Expect Pulmonary Endobronchial Ultrasound Transbronchial Aspiration Needle

K-Number: K163248 · 2017-03-27

Decision Date2017-03-27

Product CodeEOQ

Advisory CommitteeEN

DecisionSubstantially Equivalent

Device Summary

Expect Pulmonary Endobronchial Ultrasound Transbronchial Aspiration Needle is a medical device manufactured by Boston Scientific Corporation. It received FDA 510(k) clearance on 2017-03-27 under approval number K163248. The device is classified under product code EOQ. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Expect Pulmonary Endobronchial Ultrasound Transbronchial Aspiration Needle?

Expect Pulmonary Endobronchial Ultrasound Transbronchial Aspiration Needle is a medical device that received FDA 510(k) clearance on 2017-03-27. It is manufactured by Boston Scientific Corporation. The 510(k) number is K163248.

When was Expect Pulmonary Endobronchial Ultrasound Transbronchial Aspiration Needle approved by the FDA?

Expect Pulmonary Endobronchial Ultrasound Transbronchial Aspiration Needle received FDA 510(k) clearance on 2017-03-27, under approval number K163248.

What company makes Expect Pulmonary Endobronchial Ultrasound Transbronchial Aspiration Needle?

Expect Pulmonary Endobronchial Ultrasound Transbronchial Aspiration Needle is manufactured by Boston Scientific Corporation.

What is the FDA product code for Expect Pulmonary Endobronchial Ultrasound Transbronchial Aspiration Needle?

The FDA product code for Expect Pulmonary Endobronchial Ultrasound Transbronchial Aspiration Needle is EOQ.

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Related Devices (Code: EOQ)

K161656Ambu aScope 3 Regular 5.0/2.2, Ambu aScope 3 Slim 3.8/1.2, Ambu aScope 3 Large 5.8/2.8, Ambu aView MonitorAmbu A/S K152319Auris Robotic Endoscopy System (ARES)Auris Surgical Robotics, Inc. K152466Neo-Bronchoscope -Digital Video Bronchoscopy System(Rigid/Flexible)Prosurg, Inc. K171492B7 2C Occlusion BalloonSpiration, Inc. K163537Arcpoint pulmonary needle - 18 ga, Arcpoint pulmonary needle - 21 gaCovidien, LLC K162611PeriFLEXSpiration, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.