This webinar provides information on FDA's DeNovo classification process. The webinar explains how a device classified as a Class III device but has the risk level of a Class I or II device may be downclassified to its correct risk classification.

Date : 14th January 2015 to 14th January 2015

Place : United States, Fremont

Website :http://www.compliance4all.com/

Contact Person:Event Manager

Description:

This webinar provides information on FDA's DeNovo classification process. The webinar explains how a device classified as a Class III device but has the risk level of a Class I or II device may be downclassified to its correct risk classification.

This webinar provides information on FDA's DeNovo classification process. The webinar explains how a device classified as a Class III device but has the risk level of a Class I or II device may be downclassified to its correct risk classification. will be held in Fremont,United States on date 2015-01-14

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Deadline for abstracts/proposals : 13th January 2015

Keynote Speakers :

Check the event website for more details.