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FDA 510(k) Applications Submitted by INTERVENTIONAL INNOVATIONS CORP.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K964154
10/16/1996
SEGUE INFUSION CATHETER
INTERVENTIONAL INNOVATIONS CORP.
K955525
12/04/1995
FLOWER INFUSION CATHETER MODEL F-25/50, F-60/70
INTERVENTIONAL INNOVATIONS CORP.
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