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FDA 510(k)

ARTHROSCOPE-VARIOUS MODELS FIBEROPTIC

K-Number: K832341 · 1983-10-04

ApplicantKamiya Tsusan Kaisha, Ltd.
Decision Date1983-10-04
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ARTHROSCOPE-VARIOUS MODELS FIBEROPTIC is the device name listed in this FDA 510(k) record. The listed applicant is Kamiya Tsusan Kaisha, Ltd.. It received FDA 510(k) clearance on 1983-10-04 under 510(k) number K832341. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARTHROSCOPE-VARIOUS MODELS FIBEROPTIC?

ARTHROSCOPE-VARIOUS MODELS FIBEROPTIC is a medical device that received FDA 510(k) clearance on 1983-10-04. The listed applicant is Kamiya Tsusan Kaisha, Ltd.. The 510(k) number is K832341.

When did ARTHROSCOPE-VARIOUS MODELS FIBEROPTIC receive FDA 510(k) clearance?

ARTHROSCOPE-VARIOUS MODELS FIBEROPTIC received FDA 510(k) clearance on 1983-10-04, under 510(k) number K832341.

Who is the listed applicant for ARTHROSCOPE-VARIOUS MODELS FIBEROPTIC?

The FDA 510(k) record lists Kamiya Tsusan Kaisha, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ARTHROSCOPE-VARIOUS MODELS FIBEROPTIC?

The FDA product code for ARTHROSCOPE-VARIOUS MODELS FIBEROPTIC is HRX.

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Other records listing Kamiya Tsusan Kaisha, Ltd. 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.

K863161TABLE, OPERATING ROOM, HYDRAULICK832342ENDOSCOPIC CAMERA TV W/AUDIOK832340OPERATING ROOM TABLES HYDRAULIC

Related Devices (Code: HRX)

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.

K260203Fule Vertebroplasty Balloon CatheterBeijing Fule Science & Technology Development Co., Ltd.K254103HOPKINS Telescopes for ArthroscopyKarl Storz SE & CO. KGK252790Digital ClarusScope System and Digital NeuroPEN SystemClarus Medical, LLCK253523Freedom DS™ Decompression SystemSpinal SimplicityK252546VantageTM Lumbar Decompression KitAllevion Medical, LLCK253217MiiS Horus Arthroscope (EJA 100); MiiS Horus Endoscope Display System -Tablet (EDS 500); MiiS Horus Endoscope Display System -Video Box (EVS 700)Medimaging Integrated Solution, Inc (Miis)

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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