Uroplasty, Inc.
Uroplasty, Inc. holds FDA 510(k) medical device clearances, first cleared 2005, most recent 2012.
Top product codes for Uroplasty, Inc.
Recent clearances by Uroplasty, Inc.
- K121337 — UROPLASTY RIGID ENDOSCPIC NEEDLES
- K101847 — URGENT PC STIMULATOR; URGENT PC LEAD SET
- K091391 — UROPLASTY RIGID ENDOSCOPIC NEEDLE, MRN-518
- K071822 — URGENT PC NEUROMODULATION SYSTEM, MODELS UPC200 AND UPC250-12
- K061333 — URGENT PC NEUROMODULATION SYSTEM, MODELS UPC200-A AND UPC250-12
- K052025 — URGENT PC NEUROMODULATION SYSTEM
- K052175 — I-STOP MID-URETHRAL SLING, MODELS IS-1000, IS-2000, IS-3000, IS-4000
- K051905 — UROPLASTY RIGID ENDOSCOPIC NEEDLE
Data sourced from openFDA. This site is unofficial and independent of the FDA.