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FDA 510(k)

FMS ARTHOPROBE

K-Number: K955500 · 1996-02-05

ApplicantFuture Medical Systems, Inc.
Decision Date1996-02-05
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

FMS ARTHOPROBE is the device name listed in this FDA 510(k) record. The listed applicant is Future Medical Systems, Inc.. It received FDA 510(k) clearance on 1996-02-05 under 510(k) number K955500. 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 FMS ARTHOPROBE?

FMS ARTHOPROBE is a medical device that received FDA 510(k) clearance on 1996-02-05. The listed applicant is Future Medical Systems, Inc.. The 510(k) number is K955500.

When did FMS ARTHOPROBE receive FDA 510(k) clearance?

FMS ARTHOPROBE received FDA 510(k) clearance on 1996-02-05, under 510(k) number K955500.

Who is the listed applicant for FMS ARTHOPROBE?

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

What is the FDA product code for FMS ARTHOPROBE?

The FDA product code for FMS ARTHOPROBE is HRX.

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Other records listing Future Medical Systems, 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.

K023963ADHOC CLAWK021030TITANIUM CANNULATED INTERFERENCE SCREWK013685PLLA CANNULATED INTERFERENCE SCREWK002040FMS SOLOK980808ENDO FMS UROLOGYK954465FMS DUO

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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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