Home » Vascular Receives 510(k) for ThrombiGel Hemostatic Foam
Vascular Receives 510(k) for ThrombiGel Hemostatic Foam
Vascular Solutions announced that it has received 510(k) clearance by the FDA for its ThrombiGel hemostatic foam, a new version of the company's original D-Stat Dry product. The ThrombiGel version contains a gelatin foam pad (replacing the gauze pad in the original D-Stat Dry) to provide a unique, premixed, sterile, gelatin/thrombin hemostat.
MENAFN (http://menafn.com/qn_news_story.asp?StoryId=CqMmWWbWbmta4CdaWmde)
KEYWORDS FDAnews Device Daily Bulletin
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21Oct