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FDA 510(k)

FUJIFILM Video Bronchoscopes

K-Number: K182253 · 2019-04-04

ApplicantFujifilm Corporation
Decision Date2019-04-04
Product CodeEOQ
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

FUJIFILM Video Bronchoscopes is a medical device manufactured by Fujifilm Corporation. It received FDA 510(k) clearance on 2019-04-04 under approval number K182253. 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 FUJIFILM Video Bronchoscopes?

FUJIFILM Video Bronchoscopes is a medical device that received FDA 510(k) clearance on 2019-04-04. It is manufactured by Fujifilm Corporation. The 510(k) number is K182253.

When was FUJIFILM Video Bronchoscopes approved by the FDA?

FUJIFILM Video Bronchoscopes received FDA 510(k) clearance on 2019-04-04, under approval number K182253.

What company makes FUJIFILM Video Bronchoscopes?

FUJIFILM Video Bronchoscopes is manufactured by Fujifilm Corporation.

What is the FDA product code for FUJIFILM Video Bronchoscopes?

The FDA product code for FUJIFILM Video Bronchoscopes is 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.

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