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Zdrowie i gospodarka · 17/11/2010

FDA Publishes Guidance for Non-Powered Suction Apparatus Devices for Negative Pressure Wound Therapy

The FDA has released a guidance document outlining the requirements for non-powered suction apparatus devices intended for negative pressure wound therapy, which are now classified as Class II devices subject to special controls.

Source: Federal Register — Health and Human ServicesOpen original release →