以下幾種情況下需要做FDA510(K) 變更   

A change in indications for use from prescription      use to over the counter use

Addition of a new patient population

Changes to the environment of use such as from      professional use to home use or hospital use to ambulatory transport

Changes in frequency or duration of use

Change to indicate compatibility with a type of      device, component, or accessory that was not indicated as compatible with      the previously cleared device

Changes in sterilization, cleaning or disinfection

Changes in package integrity or shelf-life claims

Changes in device design

Changes to employ wireless communication

Changes in the human factors of the patient or user   interface

A change in material type, formulation or chemical      composition

Changes in the antibody, detection reagents,      critical reaction components or conjugates for in vitro diagnostic (IVD)      devices

更多美國FDA醫療器械產品注冊備案常見問題及方案解決請聯系深圳市思博達彭先生或登錄公司網站www.bccgd.com。

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