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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name Non-Variola Orthopoxvirus Real-Time Pcr Primer And Probe Set
510(k) Number K221834
Device Name Non-variola Orthopoxvirus Real-time PCR Primer and Probe Set
Applicant
Centers For Disease Control And Prevention
1600 Clifton Rd, NE
MS H24-11
ATLANTA,  GA  30329
Applicant Contact Julie Villanueva, PhD
Correspondent
Centers For Disease Control And Prevention
1600 Clifton Rd, NE
MS H24-11
ATLANTA,  GA  30329
Correspondent Contact Julie Villanueva, PhD
Classification Product Code
PBK  
Date Received06/23/2022
Decision Date 06/24/2022
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Microbiology
510k Review Panel Microbiology
Summary Summary
FDA Review Decision Summary
Type Special
Reviewed by Third Party No
Combination Product No
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