Medtronic Emergency Response Systems, Inc.

Medtronic Emergency Response Systems, Inc. holds 6 FDA 510(k) medical device clearances, first cleared 2004, most recent 2007.

Top product codes for Medtronic Emergency Response Systems, Inc.

MKJ — Cardiovascular5 devices
MSX — Cardiovascular1 device

Recent clearances by Medtronic Emergency Response Systems, Inc.

K063510 — LIFEPAK 12 DEFIBRILLATOR/MONITORCode MKJ·2007-01-26
K063119 — LIFEPAK 20 DEFIBRILLATOR/ MONITORCode MKJ·2006-12-22
K052057 — LIFEPAK 500 AUTOMATED EXTERNAL DEFIBRILLATORCode MKJ·2006-02-17
K052854 — LIFENET EXCHANGE SYSTEMCode MSX·2006-01-20
K042404 — LIFEPAK, MODEL 1000Code MKJ·2005-12-22
K041459 — LIFEPAK 12 DEFIBRILLATOR/MONITORCode MKJ·2004-07-01

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