Avinger, Inc.
Avinger, Inc. holds FDA 510(k) medical device clearances, first cleared 2009, most recent 2023.
Top product codes for Avinger, Inc.
Recent clearances by Avinger, Inc.
- K230005 — Pantheris LV Atherectomy Catheter
- K230594 — Tigereye ST CTO-Crossing Catheter
- K212468 — Tigereye CTO-Crossing Catheter
- K212047 — Pantheris System
- K201330 — Tigereye CTO-Crossing Catheter
- K182341 — Pantheris SV
- K173862 — Pantheris System
- K172236 — Pantheris Catheter (8F), Pantheris Catheter (7F), Lightbox HS Imaging Console, Lightbox Sled
- K163264 — Pantheris Catheter (8F); Pantheris Cather (7F); Lightbox HS Imaging Console; Lightbox Sled
- K162326 — Pantheris Catheter, Lightbix HS Imaging Console, Lightbox Sled
- K160827 — Pantheris Catheter
- K153460 — Pantheris Catheter (8Fr), Pantheris Catheter (7Fr)
- K152275 — Pantheris System
- K140185 — OCELOT CATHETER, OCELOT PIXL CATHETER, LIGHTBOX CONSOLE
- K123532 — OCELOT PIXL CATHETER
- K123462 — OCELOT CATHETER
- K122380 — OCELOT SYSTEM
- K120273 — KITTYCAT CATHETER, KITTYCAT 2 CATHETER
- K113838 — WILDCAT CATHETER
- K112579 — WILDCAT 5F GUIDEWIRE SUPPORT CATHETER
- K111704 — AVINGER WILDCAT 6F GUIDEWIRE SUPPORT CATHETER AND JUICEBOX
- K111338 — WILDCAT CATHETER
- K101647 — WILDCAT 5F GUIDEWIRE SUPPORT CATHETER, MODE W500
- K102022 — WILDCAT 6F GUIDEWIRE SUPPORT CATHETER MODEL W400L AND W400S
- K083313 — WILDCAT 7F GUIDEWIRE SUPPORT CATHETER
Data sourced from openFDA. This site is unofficial and independent of the FDA.