Drug news
Air Band (Maquet Cardiovascular) given FDA 510(k) and EU CE Mark approval for use in Surgery
The FDA has given 510(k) clearance for the Air Band radial compression device, from Maquet Cardiovascular. The device is indicated to assist hemostasis of the radial artery after a transradial procedure, and is designed to compress the radial artery puncture site while maintaining site visibility and a secure fit around the wrist during Surgery. Additionally, the EU has given CE Mark approval to the Air Band, which will be commercially available in the European Union later this month and in the United States in April.
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