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FDA 510(k)

FUJINON G5 BRONCHOSCOPES, MODELS EB-470S, EB-250S, AND EB-270P

K-Number: K050907 · 2005-05-19

ApplicantFujinon, Inc.
Decision Date2005-05-19
Product CodeEOQ
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

FUJINON G5 BRONCHOSCOPES, MODELS EB-470S, EB-250S, AND EB-270P is the device name listed in this FDA 510(k) record. The listed applicant is Fujinon, Inc.. It received FDA 510(k) clearance on 2005-05-19 under 510(k) number K050907. 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 FUJINON G5 BRONCHOSCOPES, MODELS EB-470S, EB-250S, AND EB-270P?

FUJINON G5 BRONCHOSCOPES, MODELS EB-470S, EB-250S, AND EB-270P is a medical device that received FDA 510(k) clearance on 2005-05-19. The listed applicant is Fujinon, Inc.. The 510(k) number is K050907.

When did FUJINON G5 BRONCHOSCOPES, MODELS EB-470S, EB-250S, AND EB-270P receive FDA 510(k) clearance?

FUJINON G5 BRONCHOSCOPES, MODELS EB-470S, EB-250S, AND EB-270P received FDA 510(k) clearance on 2005-05-19, under 510(k) number K050907.

Who is the listed applicant for FUJINON G5 BRONCHOSCOPES, MODELS EB-470S, EB-250S, AND EB-270P?

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

What is the FDA product code for FUJINON G5 BRONCHOSCOPES, MODELS EB-470S, EB-250S, AND EB-270P?

The FDA product code for FUJINON G5 BRONCHOSCOPES, MODELS EB-470S, EB-250S, AND EB-270P 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 Fujinon, 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.

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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

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

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