FDA 510(k) Applications Submitted by MIKE WINEGAR

FDA 510(k) Number Submission Date Device Name Applicant
K050073 01/12/2005 MODIFICATION TO AMPHIRION DEEP 0.014 OTW PTA BALLOON CATHETER INVATEC INNOVATIVE TECHNOLOGIES, S.R.L.
K042537 09/20/2004 SUBMARINE PLUS PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY (PTA) CATHETER, MODEL SUVXXXXXXXXX INVATEC INNOVATIVE TECHNOLOGIES
K042538 09/20/2004 SAILOR PLUS PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY (PTA) CATHETER, MODEL SAEXXXXXXXXX INVATEC INNOVATIVE TECHNOLOGIES
K042624 09/27/2004 AMPHIRION DEEP 0.014 OTW PTA BALLOON CATHETER INVATEC INNOVATIVE TECHNOLOGIES, S.R.L.


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