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FDA 510(k) Application Details - K230901
Device Classification Name
Campylobacter Pylori
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510(K) Number
K230901
Device Name
Campylobacter Pylori
Applicant
Meridian Bioscience, Inc.
3471 River Hills Drive
Cincinnati, OH 45244 US
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Contact
Heather Planck
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Regulation Number
866.3110
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Classification Product Code
LYR
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More FDA Info for this Product Code
Date Received
03/31/2023
Decision Date
07/03/2023
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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