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FDA 510(k)

IMPROVED ARTHROSCOPE

K-Number: K830120 · 1983-03-17

ApplicantMarkoptic
Decision Date1983-03-17
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

IMPROVED ARTHROSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Markoptic. It received FDA 510(k) clearance on 1983-03-17 under 510(k) number K830120. 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 IMPROVED ARTHROSCOPE?

IMPROVED ARTHROSCOPE is a medical device that received FDA 510(k) clearance on 1983-03-17. The listed applicant is Markoptic. The 510(k) number is K830120.

When did IMPROVED ARTHROSCOPE receive FDA 510(k) clearance?

IMPROVED ARTHROSCOPE received FDA 510(k) clearance on 1983-03-17, under 510(k) number K830120.

Who is the listed applicant for IMPROVED ARTHROSCOPE?

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

What is the FDA product code for IMPROVED ARTHROSCOPE?

The FDA product code for IMPROVED 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 Markoptic 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.

K860607MARKOPTIC IMPROVED ARTHROSCOPE

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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