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FDA 510(k)

ARTHROSCOPY KNIVES/PROBES/BENDING TOOL

K-Number: K831656 · 1983-06-30

ApplicantRichards Manufacturer Co.
Decision Date1983-06-30
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ARTHROSCOPY KNIVES/PROBES/BENDING TOOL is the device name listed in this FDA 510(k) record. The listed applicant is Richards Manufacturer Co.. It received FDA 510(k) clearance on 1983-06-30 under 510(k) number K831656. 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 ARTHROSCOPY KNIVES/PROBES/BENDING TOOL?

ARTHROSCOPY KNIVES/PROBES/BENDING TOOL is a medical device that received FDA 510(k) clearance on 1983-06-30. The listed applicant is Richards Manufacturer Co.. The 510(k) number is K831656.

When did ARTHROSCOPY KNIVES/PROBES/BENDING TOOL receive FDA 510(k) clearance?

ARTHROSCOPY KNIVES/PROBES/BENDING TOOL received FDA 510(k) clearance on 1983-06-30, under 510(k) number K831656.

Who is the listed applicant for ARTHROSCOPY KNIVES/PROBES/BENDING TOOL?

The FDA 510(k) record lists Richards Manufacturer Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ARTHROSCOPY KNIVES/PROBES/BENDING TOOL?

The FDA product code for ARTHROSCOPY KNIVES/PROBES/BENDING TOOL is HRX.

Related Clinical Trials

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Other records listing Richards Manufacturer Co. 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.

K831999FEMORAL CANAL SUCTION TAMPONK831884SPECTRON EXTRA-SMALL, STRAIGHT FEMORALK832000THIGH HOLDER

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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