FDA 510(k) Applications Submitted by UROPLASTY, INC.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K121337 |
05/03/2012 |
UROPLASTY RIGID ENDOSCPIC NEEDLES |
UROPLASTY, INC. |
| K061333 |
05/12/2006 |
URGENT PC NEUROMODULATION SYSTEM, MODELS UPC200-A AND UPC250-12 |
UROPLASTY, INC. |
| K071822 |
07/03/2007 |
URGENT PC NEUROMODULATION SYSTEM, MODELS UPC200 AND UPC250-12 |
UROPLASTY, INC. |
| 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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