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FDA 510(k)

ARGUS ARTHROSCOPY INSTRUMENT SYSTEM

K-Number: K950242 · 1995-05-15

ApplicantArgus Medical Co., Inc.
Decision Date1995-05-15
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ARGUS ARTHROSCOPY INSTRUMENT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Argus Medical Co., Inc.. It received FDA 510(k) clearance on 1995-05-15 under 510(k) number K950242. 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 ARGUS ARTHROSCOPY INSTRUMENT SYSTEM?

ARGUS ARTHROSCOPY INSTRUMENT SYSTEM is a medical device that received FDA 510(k) clearance on 1995-05-15. The listed applicant is Argus Medical Co., Inc.. The 510(k) number is K950242.

When did ARGUS ARTHROSCOPY INSTRUMENT SYSTEM receive FDA 510(k) clearance?

ARGUS ARTHROSCOPY INSTRUMENT SYSTEM received FDA 510(k) clearance on 1995-05-15, under 510(k) number K950242.

Who is the listed applicant for ARGUS ARTHROSCOPY INSTRUMENT SYSTEM?

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

What is the FDA product code for ARGUS ARTHROSCOPY INSTRUMENT SYSTEM?

The FDA product code for ARGUS ARTHROSCOPY INSTRUMENT SYSTEM is HRX.

Related Clinical Trials

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.

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Other records listing Argus Medical Co., 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.

K950255ARGUS HYSTEROSCOPY INSTRUMENT SYSTEMK951624ARGUS MEDICAL COMPANY LAPAROSCOPIC DISCECTOMY INSTRUMENT SYSTEMK950297ARGUS ENDOSCOPIC PLASTIC SURGERY INSTRUMENT SYSTEMK946011ARGUS SINUS ENDOSCOPY INSTRUMENT SYSTEMK950378ARGUS LAPAROSCOPY INSTRUMENT SYSTEM

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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