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FDA 510(k) Application Details - K082571
Device Classification Name
More FDA Info for this Device
510(K) Number
K082571
Device Name
AVAULTA SUPPORT SYSTEM
Applicant
C.R. BARD, INC.
13183 HARLAND DRIVE
COVINGTON, GA 30014-6421 US
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Contact
JOHN C KNORPP
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Regulation Number
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Classification Product Code
OTP
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Date Received
09/05/2008
Decision Date
09/30/2008
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
OB - Obstetrics/Gynecology
Review Advisory Committee
OB - Obstetrics/Gynecology
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
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