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# Getinge Vasoview Hemopro 3 Cleared
- URL: https://www.fdaweb.com/getinge-vasoview-hemopro-3-cleared/
- Published: 2024-03-08T12:00:00.000Z
- Updated: 2026-09-14T14:24:55.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5156512

FDA has cleared a Getinge 510(k) for the Vasoview Hemopro 3, a third-generation endoscopic vessel harvesting (EVH) device. The Vasoview Hemopro is primarily indicated for patients undergoing EVH for arterial bypass. Its 7 mm extended length endoscope and dissection tip allows for visualization of a surgical cavity, dissection and access for vessel harvesting, the company says. Extremity procedures include tissue dissection/vessel harvesting along the saphenous vein for use in coronary artery bypass grafting and peripheral artery bypass or radial artery for use in coronary artery bypass graft surgery, it adds.