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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