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FDA 510(k)

FUJINON VIDEO LAPAROSCOPE, MODIFIED

K-Number: K930297 · 1994-03-29

ApplicantFujinon, Inc.
Decision Date1994-03-29
Product CodeFWF
Advisory CommitteeSU
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 1994-03-29 under 510(k) number K930297. The device is classified under product code FWF. It was reviewed by the SU 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 1994-03-29. The listed applicant is Fujinon, Inc.. The 510(k) number is K930297.

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

FUJINON VIDEO LAPAROSCOPE, MODIFIED received FDA 510(k) clearance on 1994-03-29, under 510(k) number K930297.

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 FWF.

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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: FWF)

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.

K053412FLEXISCOPE, MODELS 50MH AND 50 MHCSchoelly Imaging, Inc.K990154KARL STORZ DIRECT COUPLED INTERFACE (DCI 5) CAMERA SYSTEMKarl Storz Imaging, Inc.K982754EC-1000-7 DIGITAL ENDOSCOPY VIDEO CAMERA, MODELS EC 1000-7P (PAL) & EC 1000-7N (NTSC)A.Stein - Regulatory Affairs ConsultingK982965ENDOCAM CAMERA SYSTEMS 5502/5507 WITH CR CAMERA HEADS AND ACCESSORIESRichard Wolf Medical Instruments Corp.K982397VES 3001-M COMPLETE VIDEO ENDOSCOPIC SYSTEMAngiolaz, Inc.K982409VES 1501-MAngiolaz, Inc.

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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