Cardima, Inc.
Cardima, Inc. holds FDA 510(k) medical device clearances, first cleared 1993, most recent 2006.
Top product codes for Cardima, Inc.
Recent clearances by Cardima, Inc.
- K060715 — MODIFICATION TO: CARDIMA ABLATION SYSTEM
- K022008 — CARDIMA ABLATION SYSTEM
- K974683 — NAVIPORT DEFLECTABLE TIP GUIDING CATHETER
- K972803 — TRACER O-T-W MAPPING DEVICE
- K982835 — ELECTRODE SWITCHBOX, MODEL 11-081002
- K971975 — CARDIMA PATHFINDER 1.5F MAPPING MICROCATHETER
- K973298 — CARDIMA VUEPORT CORONARY SINUS BALLOON OCCLUSION GUIDING CATHETER
- K970853 — PATHFINDER 3MM MAPPING MICROCATHETER (01-082001)
- K955802 — PATHFINDER
- K951603 — CARDIMA, INC. FORERUNNER
- K932800 — CARDIMA TRACKER(R) INFUSION CATHETER
- K932801 — CARDIMA SEEKER AND STUBBIE GUIDEWIRES
Data sourced from openFDA. This site is unofficial and independent of the FDA.