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FDA 510(k)

THROMBIX PATCH THROMBIN HEMOSTASIS PATCH

K-Number: K072117 · 2007-10-05

Decision Date2007-10-05
Product CodeQSX
DecisionSubstantially Equivalent

Device Summary

THROMBIX PATCH THROMBIN HEMOSTASIS PATCH is the device name listed in this FDA 510(k) record. The listed applicant is Vascular Solutions, Inc.. It received FDA 510(k) clearance on 2007-10-05 under 510(k) number K072117. The device is classified under product code QSX. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THROMBIX PATCH THROMBIN HEMOSTASIS PATCH?

THROMBIX PATCH THROMBIN HEMOSTASIS PATCH is a medical device that received FDA 510(k) clearance on 2007-10-05. The listed applicant is Vascular Solutions, Inc.. The 510(k) number is K072117.

When did THROMBIX PATCH THROMBIN HEMOSTASIS PATCH receive FDA 510(k) clearance?

THROMBIX PATCH THROMBIN HEMOSTASIS PATCH received FDA 510(k) clearance on 2007-10-05, under 510(k) number K072117.

Who is the listed applicant for THROMBIX PATCH THROMBIN HEMOSTASIS PATCH?

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

What is the FDA product code for THROMBIX PATCH THROMBIN HEMOSTASIS PATCH?

The FDA product code for THROMBIX PATCH THROMBIN HEMOSTASIS PATCH is QSX.

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 Vascular Solutions, 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.

View all 96 devices →

Related Devices (Code: QSX)

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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