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FDA 510(k)

MICRO-ARTHROSCOPE

K-Number: K930084 · 1995-09-01

ApplicantMedical Devices, Inc.
Decision Date1995-09-01
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent for Some Indications

Device Summary

MICRO-ARTHROSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Medical Devices, Inc.. It received FDA 510(k) clearance on 1995-09-01 under 510(k) number K930084. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the MICRO-ARTHROSCOPE?

MICRO-ARTHROSCOPE is a medical device that received FDA 510(k) clearance on 1995-09-01. The listed applicant is Medical Devices, Inc.. The 510(k) number is K930084.

When did MICRO-ARTHROSCOPE receive FDA 510(k) clearance?

MICRO-ARTHROSCOPE received FDA 510(k) clearance on 1995-09-01, under 510(k) number K930084.

Who is the listed applicant for MICRO-ARTHROSCOPE?

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

What is the FDA product code for MICRO-ARTHROSCOPE?

The FDA product code for MICRO-ARTHROSCOPE is HRX.

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Other records listing Medical Devices, 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.

K002280PAD PRO PEDIATRIC ELECTRODE, MODEL PAD PRO 2602K943126ELECTROFLEXK940012SMARTBRACE ELECTRODEK935132HOME MICROCURRENT HMCK934619FLEXMATEK924897XENON ENDOSCOPIC ILLUMINATOR, MODEL XEI-300

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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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