FDA Reissues Emergency Use Authorization for Non-NIOSH-Approved Filtering Facepiece Respirators
The US Food and Drug Administration (FDA) reissued the emergency use authorization (EUA) for certain filtering facepiece respirators (FFRs) that are manufactured in China and not approved by the CDC’s NIOSH.
Recognizing there is still a shortage of FFRs, the FDA is continuing the EUA for respirator models already included in Appendix A of the reissued EUA to provide additional capacity as needed. Please see the attached EUA below:
OSHA's COVID-19 webpage