FDA 510(k) Applications Submitted by MICHAEL J QUINN

FDA 510(k) Number Submission Date Device Name Applicant
K990713 03/04/1999 SPECTRANETICS LEAD LOCKING DEVICE (LLD) #1, #2, #3 LISTER SPECTRANETICS CORP.
K991059 03/30/1999 SPECTRANETICS 0.014 SUPPORT CATHETER, MODEL 518-016, SPECTRANETICS 0.018 SUPPORT CATHETER, MODEL 518-017 SPECTRANETICS CORP.


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