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FDA 510(k) Application Details - K023514
Device Classification Name
More FDA Info for this Device
510(K) Number
K023514
Device Name
TRELLIS-6 PERIPHERAL INFUSION SYSTEM (140CM CATHETER LENGTH 10CM INFUSION LENGTH)
Applicant
BACCHUS VASCULAR, INC.
3110 CORONADO DR.
SANTA CLARA, CA 95054 US
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Contact
GREGORY J MATHISON
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Regulation Number
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Classification Product Code
QEY
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Date Received
10/21/2002
Decision Date
12/02/2002
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
CV - Cardiovascular
Review Advisory Committee
CV - Cardiovascular
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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