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FDA 510(k) Application Details - K953300
Device Classification Name
Catheter,Intravascular,Therapeutic,Long-Term Greater Than 30 Days
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510(K) Number
K953300
Device Name
Catheter,Intravascular,Therapeutic,Long-Term Greater Than 30 Days
Applicant
HDC CORP.
2109 O'TOOLE AVE.
SAN JOSE, CA 95131 US
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Contact
BRUCE FIELDS
Other 510(k) Applications for this Contact
Regulation Number
880.5970
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Classification Product Code
LJS
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More FDA Info for this Product Code
Date Received
07/14/1995
Decision Date
04/30/1996
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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