FDA 510(k) Applications Submitted by WILLIAM SLEVIN

FDA 510(k) Number Submission Date Device Name Applicant
K010420 02/12/2001 RUSCH MMG/O'NEIL CATHETER RUSCH, INC.
K050918 04/12/2005 KOO AMERICAS VALVE PEEP, MODEL KM-809 KOO AMERICAS, INC.
K152340 08/19/2015 NAR Sharps Shuttle; NAR Sharps Shuttle Pack of six North American Rescue, LLC
K123194 10/11/2012 JUNCTIONAL EMERGENCY TREATMENT TOOL MODEL 30-0088 NORTH AMERICAN RESCUE PRODUCTS, INC.
K053495 12/15/2005 EQUIPMENT SLUSH DRAPE ADVANCE MEDICAL DESIGNS, INC.


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