VASCULAR SOLUTIONS DUETT FLOWABLE HEMOSTAT
K-Number: K012293 · 2002-01-18
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Device Summary
Frequently Asked Questions
What is the VASCULAR SOLUTIONS DUETT FLOWABLE HEMOSTAT?
VASCULAR SOLUTIONS DUETT FLOWABLE HEMOSTAT is a medical device that received FDA 510(k) clearance on 2002-01-18. The listed applicant is Vascular Solutions, Inc.. The 510(k) number is K012293.
When did VASCULAR SOLUTIONS DUETT FLOWABLE HEMOSTAT receive FDA 510(k) clearance?
VASCULAR SOLUTIONS DUETT FLOWABLE HEMOSTAT received FDA 510(k) clearance on 2002-01-18, under 510(k) number K012293.
Who is the listed applicant for VASCULAR SOLUTIONS DUETT FLOWABLE HEMOSTAT?
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 VASCULAR SOLUTIONS DUETT FLOWABLE HEMOSTAT?
The FDA product code for VASCULAR SOLUTIONS DUETT FLOWABLE HEMOSTAT 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.
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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