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FDA 510(k)

MTP ARTHROPUMP DISPOSABLE TUBING SET

K-Number: K990911 · 1999-06-03

ApplicantMtp Medical Technical Promotion GmbH
Decision Date1999-06-03
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MTP ARTHROPUMP DISPOSABLE TUBING SET is the device name listed in this FDA 510(k) record. The listed applicant is Mtp Medical Technical Promotion GmbH. It received FDA 510(k) clearance on 1999-06-03 under 510(k) number K990911. 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 MTP ARTHROPUMP DISPOSABLE TUBING SET?

MTP ARTHROPUMP DISPOSABLE TUBING SET is a medical device that received FDA 510(k) clearance on 1999-06-03. The listed applicant is Mtp Medical Technical Promotion GmbH. The 510(k) number is K990911.

When did MTP ARTHROPUMP DISPOSABLE TUBING SET receive FDA 510(k) clearance?

MTP ARTHROPUMP DISPOSABLE TUBING SET received FDA 510(k) clearance on 1999-06-03, under 510(k) number K990911.

Who is the listed applicant for MTP ARTHROPUMP DISPOSABLE TUBING SET?

The FDA 510(k) record lists Mtp Medical Technical Promotion GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MTP ARTHROPUMP DISPOSABLE TUBING SET?

The FDA product code for MTP ARTHROPUMP DISPOSABLE TUBING SET is HRX.

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Other records listing Mtp Medical Technical Promotion GmbH 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.

K091178MTP DISPOSABLE EQUIPMENT COVERS, KARL STORZ 15 TOUCH SCREENK021811UNIDRIVE II PLUS DISPOSABLE TUBING SETK020599MTP CLEARVISION DISPOSABLE TUBING SETK011360MTP LAPAROMAT DISPOSABLE TUBING SETK000337MTP DISPOSABLE TROCAR VALVESK994066MTP DISPOSABLE TROCARS

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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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