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FDA 510(k)

MTP DISPOSABLE EQUIPMENT COVERS, KARL STORZ 15 TOUCH SCREEN

K-Number: K091178 · 2009-07-31

Decision Date2009-07-31
Product CodeMMP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MTP DISPOSABLE EQUIPMENT COVERS, KARL STORZ 15 TOUCH SCREEN 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 2009-07-31 under 510(k) number K091178. The device is classified under product code MMP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MTP DISPOSABLE EQUIPMENT COVERS, KARL STORZ 15 TOUCH SCREEN?

MTP DISPOSABLE EQUIPMENT COVERS, KARL STORZ 15 TOUCH SCREEN is a medical device that received FDA 510(k) clearance on 2009-07-31. The listed applicant is Mtp Medical Technical Promotion GmbH. The 510(k) number is K091178.

When did MTP DISPOSABLE EQUIPMENT COVERS, KARL STORZ 15 TOUCH SCREEN receive FDA 510(k) clearance?

MTP DISPOSABLE EQUIPMENT COVERS, KARL STORZ 15 TOUCH SCREEN received FDA 510(k) clearance on 2009-07-31, under 510(k) number K091178.

Who is the listed applicant for MTP DISPOSABLE EQUIPMENT COVERS, KARL STORZ 15 TOUCH SCREEN?

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 DISPOSABLE EQUIPMENT COVERS, KARL STORZ 15 TOUCH SCREEN?

The FDA product code for MTP DISPOSABLE EQUIPMENT COVERS, KARL STORZ 15 TOUCH SCREEN is MMP.

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.

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.

View all 10 devices →

Related Devices (Code: MMP)

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.

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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