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FDA 510(k) Application Details - K030076
Device Classification Name
Tubes, Vials, Systems, Serum Separators, Blood Collection
More FDA Info for this Device
510(K) Number
K030076
Device Name
Tubes, Vials, Systems, Serum Separators, Blood Collection
Applicant
BIOMED PERSONAL METABOLIC AND NUTRITIONAL TESTING
6075 POPLAR AVE.
SUITE 500
MEMPHIS, TN 38119 US
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Contact
SUSAN B FENTRESS
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
01/08/2003
Decision Date
07/07/2003
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
CH - Clinical Chemistry
Review Advisory Committee
CH - Clinical Chemistry
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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