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FDA 510(k)

FUJIFILM Endoscope Model EB-710XT

K-Number: K240075 · 2024-02-07

ApplicantFUJIFILM Healthcare Americas Corporation
Decision Date2024-02-07
Product CodeEOQ
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

FUJIFILM Endoscope Model EB-710XT is a medical device manufactured by FUJIFILM Healthcare Americas Corporation. It received FDA 510(k) clearance on 2024-02-07 under approval number K240075. 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 Endoscope Model EB-710XT?

FUJIFILM Endoscope Model EB-710XT is a medical device that received FDA 510(k) clearance on 2024-02-07. It is manufactured by FUJIFILM Healthcare Americas Corporation. The 510(k) number is K240075.

When was FUJIFILM Endoscope Model EB-710XT approved by the FDA?

FUJIFILM Endoscope Model EB-710XT received FDA 510(k) clearance on 2024-02-07, under approval number K240075.

What company makes FUJIFILM Endoscope Model EB-710XT?

FUJIFILM Endoscope Model EB-710XT is manufactured by FUJIFILM Healthcare Americas Corporation.

What is the FDA product code for FUJIFILM Endoscope Model EB-710XT?

The FDA product code for FUJIFILM Endoscope Model EB-710XT 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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