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FDA 510(k) Application Details - K192376
Device Classification Name
More FDA Info for this Device
510(K) Number
K192376
Device Name
Simplexa VZV Swab Direct, Simplexa VZV Positive Control Pack
Applicant
DiaSorin Molecular LLC
11331 Valley View Street
Cypress, CA 90630 US
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Contact
Sharon Young
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Regulation Number
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Classification Product Code
PGI
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More FDA Info for this Product Code
Date Received
08/30/2019
Decision Date
11/26/2019
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
MI - Microbiology
Review Advisory Committee
MI - Microbiology
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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