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FDA 510(k) Application Details - K981792
Device Classification Name
Set, Administration, Intravascular
More FDA Info for this Device
510(K) Number
K981792
Device Name
Set, Administration, Intravascular
Applicant
BAXTER HEALTHCARE CORP.
RT. 120 & WILSON RD.
ROUND LAKE, IL 60073 US
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Contact
MARY ELLEN SNYDER
Other 510(k) Applications for this Contact
Regulation Number
880.5440
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Classification Product Code
FPA
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More FDA Info for this Product Code
Date Received
05/21/1998
Decision Date
08/17/1998
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
HO - General Hospital
Review Advisory Committee
HO - General Hospital
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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