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FDA 510(k)

OPTICAL CATHETER ARTHROSCOPE

K-Number: K911296 · 1991-09-24

ApplicantMedical Dynamics, Inc.
Decision Date1991-09-24
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

OPTICAL CATHETER ARTHROSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Medical Dynamics, Inc.. It received FDA 510(k) clearance on 1991-09-24 under 510(k) number K911296. 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 OPTICAL CATHETER ARTHROSCOPE?

OPTICAL CATHETER ARTHROSCOPE is a medical device that received FDA 510(k) clearance on 1991-09-24. The listed applicant is Medical Dynamics, Inc.. The 510(k) number is K911296.

When did OPTICAL CATHETER ARTHROSCOPE receive FDA 510(k) clearance?

OPTICAL CATHETER ARTHROSCOPE received FDA 510(k) clearance on 1991-09-24, under 510(k) number K911296.

Who is the listed applicant for OPTICAL CATHETER ARTHROSCOPE?

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

What is the FDA product code for OPTICAL CATHETER ARTHROSCOPE?

The FDA product code for OPTICAL CATHETER ARTHROSCOPE is HRX.

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Other records listing Medical Dynamics, 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.

K974542TRUE VISION, TRUE VISION IIK921294VIDEO ENDOSCOPE-RIGID MODIFICATIONK934682SURGICAL VIDEO CAMERA AND ACCESSORIESK930568ADAIR/VERESS NEEDLE INTRODUCER SETK915538OVER THE WIRE STONE BASKETK914315OPTICAL CATHETER INTRODUCER SETS, MODIFICATION

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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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