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FDA 510(k)

YIELD TISSUE SAMPLER

K-Number: K090853 · 2009-04-07

Decision Date2009-04-07
Product CodeEOQ
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

YIELD TISSUE SAMPLER is the device name listed in this FDA 510(k) record. The listed applicant is Broncus Technologies, Inc.. It received FDA 510(k) clearance on 2009-04-07 under 510(k) number K090853. 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 YIELD TISSUE SAMPLER?

YIELD TISSUE SAMPLER is a medical device that received FDA 510(k) clearance on 2009-04-07. The listed applicant is Broncus Technologies, Inc.. The 510(k) number is K090853.

When did YIELD TISSUE SAMPLER receive FDA 510(k) clearance?

YIELD TISSUE SAMPLER received FDA 510(k) clearance on 2009-04-07, under 510(k) number K090853.

Who is the listed applicant for YIELD TISSUE SAMPLER?

The FDA 510(k) record lists Broncus Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for YIELD TISSUE SAMPLER?

The FDA product code for YIELD TISSUE SAMPLER is EOQ.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Broncus Technologies, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 11 devices →

Related Devices (Code: EOQ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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.

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