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FDA 510(k) Application Details - K982523
Device Classification Name
Susceptibility Test Discs, Antimicrobial
More FDA Info for this Device
510(K) Number
K982523
Device Name
Susceptibility Test Discs, Antimicrobial
Applicant
OXOID, LTD.
WADE RD.
BASINGSTOKE, HAMPSHIRE RG24 8PW GB
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Contact
ANDY HOLLINGSWORTH
Other 510(k) Applications for this Contact
Regulation Number
866.1620
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Classification Product Code
JTN
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More FDA Info for this Product Code
Date Received
07/20/1998
Decision Date
09/09/1998
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
MI - Microbiology
Review Advisory Committee
MI - Microbiology
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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