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Home > Devicor touts FDA nod for its next-gen breast biopsy system

Devicor touts FDA nod for its next-gen breast biopsy system

Mass Device

The FDA approves Devicor's Mammotome revolve device, a less invasive dual vacuum-assisted biopsy system for sampling breast tissue.

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Cincinnati, Ohio-based Devicor landed FDA approval for its Mammotome revolve biopsy system, a next-generation biopsy system designed to provide high quality tissue specimens while improving the efficiency of pre-biopsy planning time.

The Mammotome system features specimen management for collecting and organizing high quality individual tissue samples in numbered, as well as specimen radiograph and pathology-ready chambers to preserve tissue integrity. The less invasive DualVac vacuum technology also helps clinicians secure larger contiguous tissue samples, according to the press release.


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