Uroplasty, Inc.
FDA 510(k) & PMA Approved Devices — 8 products
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Total Devices8
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K121337 | UROPLASTY RIGID ENDOSCPIC NEEDLES | FBK | 2012-08-03 | View |
| 510(k) | K101847 | URGENT PC STIMULATOR; URGENT PC LEAD SET | NAM | 2010-10-21 | View |
| 510(k) | K091391 | UROPLASTY RIGID ENDOSCOPIC NEEDLE, MRN-518 | FBK | 2009-06-30 | View |
| 510(k) | K071822 | URGENT PC NEUROMODULATION SYSTEM, MODELS UPC200 AND UPC250-12 | NAM | 2007-08-20 | View |
| 510(k) | K061333 | URGENT PC NEUROMODULATION SYSTEM, MODELS UPC200-A AND UPC250-12 | NAM | 2006-07-03 | View |
| 510(k) | K052025 | URGENT PC NEUROMODULATION SYSTEM | NAM | 2005-10-17 | View |
| 510(k) | K052175 | I-STOP MID-URETHRAL SLING, MODELS IS-1000, IS-2000, IS-3000, IS-4000 | OTN | 2005-10-17 | View |
| 510(k) | K051905 | UROPLASTY RIGID ENDOSCOPIC NEEDLE | FBK | 2005-08-29 | View |
No matching devices.
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