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FDA 510(k)

HYDROCISION ARTHOJET SYSTEM WITH CAUTERY AND TURBOBURR

K-Number: K020688 · 2002-04-03

ApplicantHydrocision, Inc.
Decision Date2002-04-03
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

HYDROCISION ARTHOJET SYSTEM WITH CAUTERY AND TURBOBURR is the device name listed in this FDA 510(k) record. The listed applicant is Hydrocision, Inc.. It received FDA 510(k) clearance on 2002-04-03 under 510(k) number K020688. 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 HYDROCISION ARTHOJET SYSTEM WITH CAUTERY AND TURBOBURR?

HYDROCISION ARTHOJET SYSTEM WITH CAUTERY AND TURBOBURR is a medical device that received FDA 510(k) clearance on 2002-04-03. The listed applicant is Hydrocision, Inc.. The 510(k) number is K020688.

When did HYDROCISION ARTHOJET SYSTEM WITH CAUTERY AND TURBOBURR receive FDA 510(k) clearance?

HYDROCISION ARTHOJET SYSTEM WITH CAUTERY AND TURBOBURR received FDA 510(k) clearance on 2002-04-03, under 510(k) number K020688.

Who is the listed applicant for HYDROCISION ARTHOJET SYSTEM WITH CAUTERY AND TURBOBURR?

The FDA 510(k) record lists Hydrocision, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HYDROCISION ARTHOJET SYSTEM WITH CAUTERY AND TURBOBURR?

The FDA product code for HYDROCISION ARTHOJET SYSTEM WITH CAUTERY AND TURBOBURR is HRX.

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Other records listing Hydrocision, Inc. as applicant

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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

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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