THROMBI-PASTE THROMBIN/GELATIN POWDER PASTE HEMOSTAT
K-Number: K070938 · 2007-08-06
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Device Summary
Frequently Asked Questions
What is the THROMBI-PASTE THROMBIN/GELATIN POWDER PASTE HEMOSTAT?
THROMBI-PASTE THROMBIN/GELATIN POWDER PASTE HEMOSTAT is a medical device that received FDA 510(k) clearance on 2007-08-06. The listed applicant is Vascular Solutions, Inc.. The 510(k) number is K070938.
When did THROMBI-PASTE THROMBIN/GELATIN POWDER PASTE HEMOSTAT receive FDA 510(k) clearance?
THROMBI-PASTE THROMBIN/GELATIN POWDER PASTE HEMOSTAT received FDA 510(k) clearance on 2007-08-06, under 510(k) number K070938.
Who is the listed applicant for THROMBI-PASTE THROMBIN/GELATIN POWDER PASTE 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 THROMBI-PASTE THROMBIN/GELATIN POWDER PASTE HEMOSTAT?
The FDA product code for THROMBI-PASTE THROMBIN/GELATIN POWDER PASTE 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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