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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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