FDA 510(k) Applications Submitted by SUREFIRE MEDICAL, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K140034 01/07/2014 SUREFIRE GUIDING CATHETER SUREFIRE MEDICAL, INC.
K180677 03/15/2018 Surefire Spark Infusion System Surefire Medical, Inc.
K171355 05/09/2017 Surefire Precision Infusion System Surefire Medical, Inc.
K162359 08/23/2016 Surefire Guiding Catheter Surefire Medical, Inc.
K121677 06/07/2012 SUREFIRE HI-FLOW MICROCATHETER SUREFIRE MEDICAL, INC.


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