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Home » Casio Obtains 510(K) Clearance for its Dermocamera and Scope for Skin Monitoring
Casio Obtains 510(K) Clearance for its Dermocamera and Scope for Skin Monitoring
Casio America has received the FDA’s 510(k) clearance for its DZ-D100 Dermocamera and DZ-S50 scope for skin observation.
The DZ-D100 camera, which can be used to take both standard-sized and close-up images of an affected area, uses the company’s DZ Image Viewer software to manage the captured images.
The DZ-D100 and DZ-S50 have been classified by the FDA as Class I devices, meaning they pose low or moderate risk to patient health and safety.
The Dover, N.J.-based subsidiary of Japanese tech giant Casio Computer said that it plans to make the devices available in the U.S. by March.
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