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FDA 510(k)

THROMBIX 3X3 HEMOSTATIC PAD

K-Number: K053054 · 2005-11-23

Decision Date2005-11-23
Product CodeQSX
DecisionSubstantially Equivalent

Device Summary

THROMBIX 3X3 HEMOSTATIC PAD 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 2005-11-23 under 510(k) number K053054. The device is classified under product code QSX. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THROMBIX 3X3 HEMOSTATIC PAD?

THROMBIX 3X3 HEMOSTATIC PAD is a medical device that received FDA 510(k) clearance on 2005-11-23. The listed applicant is Vascular Solutions, Inc.. The 510(k) number is K053054.

When did THROMBIX 3X3 HEMOSTATIC PAD receive FDA 510(k) clearance?

THROMBIX 3X3 HEMOSTATIC PAD received FDA 510(k) clearance on 2005-11-23, under 510(k) number K053054.

Who is the listed applicant for THROMBIX 3X3 HEMOSTATIC PAD?

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 3X3 HEMOSTATIC PAD?

The FDA product code for THROMBIX 3X3 HEMOSTATIC PAD 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

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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