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FDA 510(k) Application Details - K964966
Device Classification Name
Catheter,Intravascular,Therapeutic,Short-Term Less Than 30 Days
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510(K) Number
K964966
Device Name
Catheter,Intravascular,Therapeutic,Short-Term Less Than 30 Days
Applicant
HDC CORP.
2109 O'TOOLE AVE.
SAN JOSE, CA 95131 US
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Contact
GRETCHEN MARCHESANI
Other 510(k) Applications for this Contact
Regulation Number
880.5200
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Classification Product Code
FOZ
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More FDA Info for this Product Code
Date Received
12/11/1996
Decision Date
03/05/1997
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
HO - General Hospital
Review Advisory Committee
HO - General Hospital
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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