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FDA 510(k)

FUJINON VIDEO LAPAROSCOPE--THORACOSCOPY

K-Number: K931223 · 1993-07-28

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

Device Summary

FUJINON VIDEO LAPAROSCOPE--THORACOSCOPY 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 K931223. 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--THORACOSCOPY?

FUJINON VIDEO LAPAROSCOPE--THORACOSCOPY 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 K931223.

When did FUJINON VIDEO LAPAROSCOPE--THORACOSCOPY receive FDA 510(k) clearance?

FUJINON VIDEO LAPAROSCOPE--THORACOSCOPY received FDA 510(k) clearance on 1993-07-28, under 510(k) number K931223.

Who is the listed applicant for FUJINON VIDEO LAPAROSCOPE--THORACOSCOPY?

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--THORACOSCOPY?

The FDA product code for FUJINON VIDEO LAPAROSCOPE--THORACOSCOPY is GCJ.

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Other records listing Fujinon, Inc. as applicant

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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: 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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