FDA 510(k) Application Details - K962751

Device Classification Name Port & Catheter, Implanted, Subcutaneous, Intravascular

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510(K) Number K962751
Device Name Port & Catheter, Implanted, Subcutaneous, Intravascular
Applicant IDEAS FOR MEDICINE, INC.
12167 49TH ST. NORTH
P.O. BOX 17327
CLEARWATER, FL 34622 US
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Contact ELIZABETH M PAUL
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Regulation Number 880.5965

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Classification Product Code LJT
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Date Received 07/15/1996
Decision Date 09/30/1996
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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