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15 December 2010

Comments

Philip Needham

Hi Nancy,
Each manufacturer/supplier has a copy of their 510(k)s so how about the FDA issuing us with a standard spreadsheet to us to transfer the information onto, so that it becomes searchable. Add severe penalties for misrepresenation, to keep quality high, and we would create the searchable database the FDA needs, cost is distributed across all Companies, more efficient than if the FDA attempts to do this.
Just an idea?

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