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FDA 510(k)

FUJINON EVL-F

K-Number: K912859 · 1992-01-23

ApplicantFujinon, Inc.
Decision Date1992-01-23
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

FUJINON EVL-F is the device name listed in this FDA 510(k) record. The listed applicant is Fujinon, Inc.. It received FDA 510(k) clearance on 1992-01-23 under 510(k) number K912859. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FUJINON EVL-F?

FUJINON EVL-F is a medical device that received FDA 510(k) clearance on 1992-01-23. The listed applicant is Fujinon, Inc.. The 510(k) number is K912859.

When did FUJINON EVL-F receive FDA 510(k) clearance?

FUJINON EVL-F received FDA 510(k) clearance on 1992-01-23, under 510(k) number K912859.

Who is the listed applicant for FUJINON EVL-F?

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

What is the FDA product code for FUJINON EVL-F?

The FDA product code for FUJINON EVL-F is GCJ.

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Other records listing Fujinon, Inc. 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: GCJ)

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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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