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510(k) Registration of Medical Devices

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FAQ # 01

At #8C, we wanted to start a new initiative of creating a š¬šžš«š¢šžš¬ šØšŸ š…š€šš¬, dealing with medical devices and its regulations. In that effort, here is the š’‡š’Šš’“š’”š’• š‘­š‘Øš‘ø. Hope you like these #titbits of information. Here is #FAQ01 on holding š¦š®š„š­š¢š©š„šž š¢š¦š©šØš«š­ š„š¢šœšžš§š¬šžš¬

CDSCO made iso 13485 certificate mandatory documents

The Gazette Notification, released on 18th Jan 2022, gave a provision for #Registration_Listings, for newly regulated Medical Devices

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