D-STAT DRY HEMOSTATIC BANDAGE
K-Number: K061219 · 2006-10-06
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Device Summary
Frequently Asked Questions
What is the D-STAT DRY HEMOSTATIC BANDAGE?
D-STAT DRY HEMOSTATIC BANDAGE is a medical device that received FDA 510(k) clearance on 2006-10-06. The listed applicant is Vascular Solutions, Inc.. The 510(k) number is K061219.
When did D-STAT DRY HEMOSTATIC BANDAGE receive FDA 510(k) clearance?
D-STAT DRY HEMOSTATIC BANDAGE received FDA 510(k) clearance on 2006-10-06, under 510(k) number K061219.
Who is the listed applicant for D-STAT DRY HEMOSTATIC BANDAGE?
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 D-STAT DRY HEMOSTATIC BANDAGE?
The FDA product code for D-STAT DRY HEMOSTATIC BANDAGE 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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