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FDA 510(k) Applications Submitted by SUREFIRE MEDICAL, INC
FDA 510(k) Number
Submission Date
Device Name
Applicant
K110459
02/17/2011
SUREFIRE INFUSION CATHETER SYSTEM
SUREFIRE MEDICAL, INC
K160662
03/09/2016
Surefire Infusion System
SUREFIRE MEDICAL, INC
K143588
12/18/2014
Surefire Infusion System 021
SUREFIRE MEDICAL, INC
K122506
08/17/2012
SUREFIRE HIGH FLOW ANGIOGRAPHIC CATHETER, ACCESS
SUREFIRE MEDICAL, INC
K113737
12/20/2011
SUREFIRE GUIDE SHEATH
SUREFIRE MEDICAL, INC
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