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FDA 510(k) Application Details - K082472
Device Classification Name
Device, Specimen Collection
More FDA Info for this Device
510(K) Number
K082472
Device Name
Device, Specimen Collection
Applicant
MEDICAL WIRE & EQUIPMENT COMPANY (BATH) LTD
POTLEY LANE
CORSHAM, WILTSHIRE SN13 9RT GB
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Contact
DAVID ELLIS
Other 510(k) Applications for this Contact
Regulation Number
866.2900
More FDA Info for this Regulation Number
Classification Product Code
LIO
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
08/28/2008
Decision Date
12/30/2008
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
MI - Microbiology
Review Advisory Committee
MI - Microbiology
Statement / Summary / Purged Status
Summary
Type
Abbreviated
Reviewed By Third Party
N
Expedited Review
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