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FDA 510(k)

FUJIFILM Endoscope Model EC-760Z-V/L

K-Number: K192664 · 2019-11-20

Decision Date2019-11-20
Product CodeFDF
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

FUJIFILM Endoscope Model EC-760Z-V/L is the device name listed in this FDA 510(k) record. The listed applicant is Fujifilm Corporation. It received FDA 510(k) clearance on 2019-11-20 under 510(k) number K192664. 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-760Z-V/L?

FUJIFILM Endoscope Model EC-760Z-V/L is a medical device that received FDA 510(k) clearance on 2019-11-20. The listed applicant is Fujifilm Corporation. The 510(k) number is K192664.

When did FUJIFILM Endoscope Model EC-760Z-V/L receive FDA 510(k) clearance?

FUJIFILM Endoscope Model EC-760Z-V/L received FDA 510(k) clearance on 2019-11-20, under 510(k) number K192664.

Who is the listed applicant for FUJIFILM Endoscope Model EC-760Z-V/L?

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

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

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

Other records listing Fujifilm Corporation 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: FDF)

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.