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FDA 510(k)

FUJINON VIDEO LAPAROSCOPE -- MODIFIED

K-Number: K932312 · 1994-02-16

ApplicantFujinon, Inc.
Decision Date1994-02-16
Product CodeFET
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

FUJINON VIDEO LAPAROSCOPE -- MODIFIED is the device name listed in this FDA 510(k) record. The listed applicant is Fujinon, Inc.. It received FDA 510(k) clearance on 1994-02-16 under 510(k) number K932312. The device is classified under product code FET. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FUJINON VIDEO LAPAROSCOPE -- MODIFIED?

FUJINON VIDEO LAPAROSCOPE -- MODIFIED is a medical device that received FDA 510(k) clearance on 1994-02-16. The listed applicant is Fujinon, Inc.. The 510(k) number is K932312.

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

FUJINON VIDEO LAPAROSCOPE -- MODIFIED received FDA 510(k) clearance on 1994-02-16, under 510(k) number K932312.

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

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 -- MODIFIED?

The FDA product code for FUJINON VIDEO LAPAROSCOPE -- MODIFIED is FET.

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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: FET)

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.

K2620794K Camera Head OLYMPUS CH-S700-08-LBOlympus Medical Systems Corp.K261880FUJIFILM Processor EP-8000;Balloon Controller PB-30;Endoscopy Support Program EW10-VM01Fujifilm CorporationK261260HD Camera Head OLYMPUS CH-S200-08-LBOlympus Medical Systems CorporationK251734ProVee Video Processing Unit (PV-003)Proverum LimitedK250462UL UHD-Clear View 4K Camera System (UL-3Chip 4K)Univlabs Technologies Private LimitedK250204Endoscopic Camera SystemShenzhen Sophway Technology Co., Ltd.

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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