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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name human metapneumovirus (hmpv) rna assay system
510(k) Number K082688
Device Name PRO HMPV+ ASSAY
Applicant
PRODESSE, INC.
W229 N1870 WESTWOOD DR.
WAUKESHA,  WI  53186
Applicant Contact KAREN HARRINGTON
Correspondent
PRODESSE, INC.
W229 N1870 WESTWOOD DR.
WAUKESHA,  WI  53186
Correspondent Contact KAREN HARRINGTON
Regulation Number866.3980
Classification Product Code
OEM  
Date Received09/15/2008
Decision Date 11/07/2008
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Microbiology
510k Review Panel Microbiology
Summary Summary
FDA Review Decision Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
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