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FDA 510(k) Application Details - K964144
Device Classification Name
Device, Specimen Collection
More FDA Info for this Device
510(K) Number
K964144
Device Name
Device, Specimen Collection
Applicant
PARA SCIENTIFIC CO.
17170 WALL ST.
LAKE OSWEGO, OR 97034 US
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Contact
ERIC CARLSON
Other 510(k) Applications for this Contact
Regulation Number
866.2900
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Classification Product Code
LIO
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More FDA Info for this Product Code
Date Received
10/17/1996
Decision Date
11/27/1996
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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