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FDA 510(k)

MTP DISPOSABLE TROCARS

K-Number: K994066 · 2000-01-20

Decision Date2000-01-20
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MTP DISPOSABLE TROCARS 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 2000-01-20 under 510(k) number K994066. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MTP DISPOSABLE TROCARS?

MTP DISPOSABLE TROCARS is a medical device that received FDA 510(k) clearance on 2000-01-20. The listed applicant is Mtp Medical Technical Promotion GmbH. The 510(k) number is K994066.

When did MTP DISPOSABLE TROCARS receive FDA 510(k) clearance?

MTP DISPOSABLE TROCARS received FDA 510(k) clearance on 2000-01-20, under 510(k) number K994066.

Who is the listed applicant for MTP DISPOSABLE TROCARS?

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 TROCARS?

The FDA product code for MTP DISPOSABLE TROCARS is GCJ.

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: GCJ)

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

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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