| The U.S. Food and Drug Administration (FDA) is announcing a meeting of the General and Plastic Surgery Devices Panel of the Medical Devices Advisory Committee. Registration is not required to attend. During this advisory committee meeting, the committee will discuss the topic of skin lesion analyzer technology and its application to detecting skin cancers in various patient care settings. The committee will also discuss the potential reclassification of approved computer-aided melanoma detection class III devices. - Virtual Workshop Date:
- July 28, 2022, from 9:00 a.m. ET to 5:45 p.m. ET
- July 29, 2022, from 9:00 a.m. ET to 4:00 p.m. ET
- Location: The meeting will be held by webcast only
Important Deadlines: - July 11: Submit comments for advisory committee consideration
- July 21: Request special accommodations for the advisory committee meeting
- August 29: Submit comments on this meeting to regulations.gov under docket number FDA-2022-N-0589
Questions? If you have questions about this advisory committee meeting, email Candace.Nalls@fda.hhs.gov. | | | |
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