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Home » Icare USA’s iCare Home2 Self-Tonometer Wins FDA’s 510(k) Clearance
Icare USA’s iCare Home2 Self-Tonometer Wins FDA’s 510(k) Clearance
Icare USA has received the FDA’s 510(k) clearance for its iCare Home2 self-tonometer, a device for measuring glaucoma patients’ intraocular pressure.
Most patients can use the device on their own by following the interactive display screen, the Raleigh, N.C.-based company says. The device lets patients take measurements while they are supine, reclining or sitting.
The tonometer uploads the intraocular pressure data to the company’s cloud-based iCare Clinic, which sends it to healthcare professionals for review.
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