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 the device name listed in this FDA 510(k) record. The listed applicant is Boston Scientific Corporation. It received FDA 510(k) clearance on 2017-03-27 under 510(k) 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. The listed applicant is Boston Scientific Corporation. The 510(k) number is K163248.

When did Expect Pulmonary Endobronchial Ultrasound Transbronchial Aspiration Needle receive FDA 510(k) clearance?

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

Who is the listed applicant for Expect Pulmonary Endobronchial Ultrasound Transbronchial Aspiration Needle?

The FDA 510(k) record lists Boston Scientific Corporation as the applicant. This does not by itself establish the device manufacturer.

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)

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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.