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FDA 510(k)

FUJINON VIDEO LAPAROSCOPE-ADDITIONAL INTENDED USE

K-Number: K925599 · 1993-07-28

ApplicantFujinon, Inc.
Decision Date1993-07-28
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

FUJINON VIDEO LAPAROSCOPE-ADDITIONAL INTENDED USE is the device name listed in this FDA 510(k) record. The listed applicant is Fujinon, Inc.. It received FDA 510(k) clearance on 1993-07-28 under 510(k) number K925599. 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 VIDEO LAPAROSCOPE-ADDITIONAL INTENDED USE?

FUJINON VIDEO LAPAROSCOPE-ADDITIONAL INTENDED USE is a medical device that received FDA 510(k) clearance on 1993-07-28. The listed applicant is Fujinon, Inc.. The 510(k) number is K925599.

When did FUJINON VIDEO LAPAROSCOPE-ADDITIONAL INTENDED USE receive FDA 510(k) clearance?

FUJINON VIDEO LAPAROSCOPE-ADDITIONAL INTENDED USE received FDA 510(k) clearance on 1993-07-28, under 510(k) number K925599.

Who is the listed applicant for FUJINON VIDEO LAPAROSCOPE-ADDITIONAL INTENDED USE?

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 VIDEO LAPAROSCOPE-ADDITIONAL INTENDED USE?

The FDA product code for FUJINON VIDEO LAPAROSCOPE-ADDITIONAL INTENDED USE is GCJ.

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Other records listing Fujinon, Inc. as applicant

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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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