Cardiosonix, Ltd.

Cardiosonix, Ltd. holds 3 FDA 510(k) medical device clearances, first cleared 2002, most recent 2004.

Top product codes for Cardiosonix, Ltd.

DPW — Cardiovascular3 devices

Recent clearances by Cardiosonix, Ltd.

K041180 — QUANTIX OR VESSEL STABILIZER DEVICECode DPW·2004-06-07
K030357 — QUANTIX/OR DEVICECode DPW·2003-08-20
K023431 — QUANTIX/ND DEVICECode DPW·2002-11-13

Data sourced from openFDA. This site is unofficial and independent of the FDA.