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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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