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FDA 510(k)

FUJIFILM Endoscope Model EC-760S-V/L

K-Number: K190649 · 2019-05-07

ApplicantFujifilm Corporation
Decision Date2019-05-07
Product CodeFDF
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

FUJIFILM Endoscope Model EC-760S-V/L is a medical device manufactured by Fujifilm Corporation. It received FDA 510(k) clearance on 2019-05-07 under approval number K190649. The device is classified under product code FDF. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FUJIFILM Endoscope Model EC-760S-V/L?

FUJIFILM Endoscope Model EC-760S-V/L is a medical device that received FDA 510(k) clearance on 2019-05-07. It is manufactured by Fujifilm Corporation. The 510(k) number is K190649.

When was FUJIFILM Endoscope Model EC-760S-V/L approved by the FDA?

FUJIFILM Endoscope Model EC-760S-V/L received FDA 510(k) clearance on 2019-05-07, under approval number K190649.

What company makes FUJIFILM Endoscope Model EC-760S-V/L?

FUJIFILM Endoscope Model EC-760S-V/L is manufactured by Fujifilm Corporation.

What is the FDA product code for FUJIFILM Endoscope Model EC-760S-V/L?

The FDA product code for FUJIFILM Endoscope Model EC-760S-V/L is FDF.

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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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