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FDA 510(k)

MEDSCOPE 4MM ARTHROSCOPE

K-Number: K894303 · 1989-07-25

ApplicantMedscope Corp.
Decision Date1989-07-25
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MEDSCOPE 4MM ARTHROSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Medscope Corp.. It received FDA 510(k) clearance on 1989-07-25 under 510(k) number K894303. 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 MEDSCOPE 4MM ARTHROSCOPE?

MEDSCOPE 4MM ARTHROSCOPE is a medical device that received FDA 510(k) clearance on 1989-07-25. The listed applicant is Medscope Corp.. The 510(k) number is K894303.

When did MEDSCOPE 4MM ARTHROSCOPE receive FDA 510(k) clearance?

MEDSCOPE 4MM ARTHROSCOPE received FDA 510(k) clearance on 1989-07-25, under 510(k) number K894303.

Who is the listed applicant for MEDSCOPE 4MM ARTHROSCOPE?

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

What is the FDA product code for MEDSCOPE 4MM ARTHROSCOPE?

The FDA product code for MEDSCOPE 4MM ARTHROSCOPE 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 Medscope Corp. 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.

K903663MEDSCOPE 8MM AND 10MM LAPAROSCOPE

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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