American Medical Systems
American Medical Systems holds FDA 510(k) medical device clearances, first cleared 2008, most recent 2014.
Top product codes for American Medical Systems
Recent clearances by American Medical Systems
- K140679 — SUREFLEX LITHOTRIPSY LASER FIBERS
- K131229 — SPARC SYSTEM AND MONARC, MONARC, AND MONARC C SYSTEMS
- K121805 — AMS LARGE PORE POLYPROPHLENE MESH
- K121641 — MINIARC PRO SINGLE-INCISION SLING SYSTEM
- K121612 — ELEVATE PROLAPSE REPAIR SYSTEMS-APICAL NEEDLE PASSER SHEATH MODIFICATION
- K120870 — GREENLIGHT MOXY FIBER OPTIC
- K111118 — AMS ELEVATE PC APICAL AND POSTERIOR ( AND ANTERIOR AND APICAL) PROLAPSE REPAIR SYSTEM WITH INTEPRO LITE
- K100746 — FIBER ONE
- K082387 — APOGEE AND PERIGEE SYSTEMS WITH INTEPRO LITE AND INTEXEN LP, PART OF THE AMS; PELVIC FLOOR REPAIR SYSTEM
- K081710 — APOGEE AND PERIGEE SYSTEMS WITH PC COATED INTEPRO LITE
Data sourced from openFDA. This site is unofficial and independent of the FDA.