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FDA 510(k) Application Details - K022875
Device Classification Name
Tubes, Vials, Systems, Serum Separators, Blood Collection
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510(K) Number
K022875
Device Name
Tubes, Vials, Systems, Serum Separators, Blood Collection
Applicant
BECTON DICKINSON & CO.
1 BECTON DR.
FRANKLIN LAKES, NJ 07417-1880 US
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Contact
M. WENDY BOSSHARDT
Other 510(k) Applications for this Contact
Regulation Number
862.1675
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Classification Product Code
JKA
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More FDA Info for this Product Code
Date Received
08/30/2002
Decision Date
09/11/2002
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
CH - Clinical Chemistry
Review Advisory Committee
CH - Clinical Chemistry
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
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