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FDA 510(k) Application Details - K051713
Device Classification Name
More FDA Info for this Device
510(K) Number
K051713
Device Name
JBAIDS ANTHRAC DETECTION SYSTEM
Applicant
IDAHO TECHNOLOGY, INC.
390 Wakara Way
Salt Lake City, UT 84108 US
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Contact
BETH LINGENFELTER
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Regulation Number
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Classification Product Code
NHT
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Date Received
06/27/2005
Decision Date
11/18/2005
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
Y
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