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Mercury Medical is thrilled to announce that the BiWaze® Clear System has received FDA 510(k) clearance for in-line ventilator use in acute care settings. This clearance marks a significant milestone in our commitment to delivering innovative solutions for healthcare professionals and patients alike.

The BiWaze® Clear System developed and manufactured by ABM Respiratory Care®, provides oscillating lung expansion (OLE) therapy to help treat and prevent atelectasis, remove retained secretions from deep in the lungs and reduce the work of breathing.

With the FDA clearance for in-line use in acute care, healthcare providers can now confidently integrate the BiWaze Clear System into their patient care protocols, enhancing efficiency and improving patient outcomes. This achievement reinforces our commitment to delivering clinically differentiated critical care technology that saves lives throughout the world.

If you would like to learn more about the BiWaze Clear System, visit the product page, or schedule a quick and easy virtual demonstration.

Read ABM’s full press release.

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