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FDA 510(k)

FUJINON VIDEO LAPORASCOPE

K-Number: K933544 · 1995-04-27

ApplicantFujinon, Inc.
Decision Date1995-04-27
Product CodeHIH
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

FUJINON VIDEO LAPORASCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Fujinon, Inc.. It received FDA 510(k) clearance on 1995-04-27 under 510(k) number K933544. The device is classified under product code HIH. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FUJINON VIDEO LAPORASCOPE?

FUJINON VIDEO LAPORASCOPE is a medical device that received FDA 510(k) clearance on 1995-04-27. The listed applicant is Fujinon, Inc.. The 510(k) number is K933544.

When did FUJINON VIDEO LAPORASCOPE receive FDA 510(k) clearance?

FUJINON VIDEO LAPORASCOPE received FDA 510(k) clearance on 1995-04-27, under 510(k) number K933544.

Who is the listed applicant for FUJINON VIDEO LAPORASCOPE?

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 LAPORASCOPE?

The FDA product code for FUJINON VIDEO LAPORASCOPE is HIH.

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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.

K120446FUJINON/FUJIFILM ULTRASONIC ENDOSCOPE EG-530UR2 AND EG-530UT2K112391FUJINON COLONOSCOPESK102466FUJINON EPX-4440HD DIGITAL VIDEO PROCESSORK111243FUJINON ULTRASONIC PROCESSORK091773FUJINON STERILE OVERTUBESK090116FUJINON COLONOSCOPE FOR DOUBLE BALLOON ENTERSCOPY SYSTEM MODEL, EC-450B15

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Related Devices (Code: HIH)

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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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