FDA 510(k) Applications Submitted by MICHAEL MORRELL

FDA 510(k) Number Submission Date Device Name Applicant
K091391 05/11/2009 UROPLASTY RIGID ENDOSCOPIC NEEDLE, MRN-518 UROPLASTY, INC.
K101847 07/01/2010 URGENT PC STIMULATOR; URGENT PC LEAD SET UROPLASTY, INC.
K051905 07/14/2005 UROPLASTY RIGID ENDOSCOPIC NEEDLE UROPLASTY, INC.
K052025 07/27/2005 URGENT PC NEUROMODULATION SYSTEM UROPLASTY, INC.
K052175 08/10/2005 I-STOP MID-URETHRAL SLING, MODELS IS-1000, IS-2000, IS-3000, IS-4000 UROPLASTY, INC.


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