Aerogen (Ireland), Ltd.

Aerogen (Ireland), Ltd. holds 3 FDA 510(k) medical device clearances, first cleared 2007, most recent 2010.

Name variants for Aerogen (Ireland), Ltd.

as filed with FDA

Aerogen (Ireland), Ltd.2 devices
Aerogen Ireland, Ltd.1 device

Top product codes for Aerogen (Ireland), Ltd.

CAF — Anesthesiology3 devices

Recent clearances by Aerogen (Ireland), Ltd.

K102240 — NIVO NEBULIZER SYSTEMCode CAF·2010-11-10
K081650 — AERONEB GO NEBULIZERCode CAF·2008-10-23
K070642 — AERONEB PROFESSIONAL NEBULIZER SYSTEMCode CAF·2007-05-07

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