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FDA 510(k)

MTP HAMOU ENDOMAT DISPOSABLE TUBING SETS

K-Number: K990910 · 1999-06-03

ApplicantMtp Medical Technical Promotion GmbH
Decision Date1999-06-03
Product CodeHIH
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MTP HAMOU ENDOMAT DISPOSABLE TUBING SETS 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 K990910. The device is classified under product code HIH. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MTP HAMOU ENDOMAT DISPOSABLE TUBING SETS?

MTP HAMOU ENDOMAT DISPOSABLE TUBING SETS 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 K990910.

When did MTP HAMOU ENDOMAT DISPOSABLE TUBING SETS receive FDA 510(k) clearance?

MTP HAMOU ENDOMAT DISPOSABLE TUBING SETS received FDA 510(k) clearance on 1999-06-03, under 510(k) number K990910.

Who is the listed applicant for MTP HAMOU ENDOMAT DISPOSABLE TUBING SETS?

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 HAMOU ENDOMAT DISPOSABLE TUBING SETS?

The FDA product code for MTP HAMOU ENDOMAT DISPOSABLE TUBING SETS is HIH.

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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: HIH)

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.

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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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