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FDA 510(k)

FUJIFILM Endoscope Model EB-710P

K-Number: K220957 · 2022-11-10

ApplicantFujifilm Corporaton
Decision Date2022-11-10
Product CodeEOQ
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

FUJIFILM Endoscope Model EB-710P is a medical device manufactured by Fujifilm Corporaton. It received FDA 510(k) clearance on 2022-11-10 under approval number K220957. 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-710P?

FUJIFILM Endoscope Model EB-710P is a medical device that received FDA 510(k) clearance on 2022-11-10. It is manufactured by Fujifilm Corporaton. The 510(k) number is K220957.

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

FUJIFILM Endoscope Model EB-710P received FDA 510(k) clearance on 2022-11-10, under approval number K220957.

What company makes FUJIFILM Endoscope Model EB-710P?

FUJIFILM Endoscope Model EB-710P is manufactured by Fujifilm Corporaton.

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

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