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Surgical Masks - Premarket Notification [510(k ...

This guidance supersedes “Draft Guidance for Industry and FDA Reviewers on the Content and Format of Premarket Notification [510(k)] Submissions for Surgical Mask” issued January 16, 1998.

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(Mask, Surgical) - FDA 510(k) Applications Database

Searchable database of FDA 510(k) applications and descisions. FDA 510(k) Applications for Medical Device Product Code "FXX" (Mask, Surgical)

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510(k) Premarket Notification

A 510(K) is a premarket submission made to FDA to demonstrate that the device to be marketed is as safe and effective, that is, substantially equivalent, to a legally marketed device (section 513(i)(1)(A) FD&C Act) that is not subject to premarket approval.

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Mar 16, 2016 · Face Mask Performance: Are You Protected? March 16, 2016 by John A. Molinari, PhD; Peri Nelson, BS Published reports in the 1960s investigated reported increases in upper respiratory tract infections in dentists from airborne splashes, spatter, and …

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