American Medical Systems
FDA 510(k) medical device clearances.
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.