Apologies for the spam, I hit the wrong button on the moderation pane.

Alan G.

On 16/02/18 13:49, Webcompliancepanel wrote:
>    [1]A Regulatory Perspective: FDA's                            [2]OCP_Logo
>    New Guidance's Deciding When to      Call 510-857-5896
>    Submit a 510(k) for Device &         38780 Tyson Lane Suite 210 Fremont,
>    Software Changes                     CA-94536
>    LIVE WEBINAR
>    Date: Monday, 12 March 2018
>    Time: 10:00 AM PDT | 01:00 PM EDT

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