FDA.reportPublic FDA data

PHYSIO-CONTROL MAASTRICHT, INC.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30100303553010030355PHYSIO-CONTROL MAASTRICHT, INC.1N2026-01-01Gaetano Martinolaan 50 Maastricht Limburg NL 6229 GS

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
2209761849399444P170018LIFEPAK® CR2 DefibrillatorMKJ2018-12-21
2209761059326393P160026LIFEPAK 1000 DEFIBRILLATOR, LIFEPAK 20 DEFIBRILLATOR/ MONITOR, LIFEPAK 20E DEFIBRILLATOR/ MONITOR, LIFEPAK 15 MONITOR/DEMKJ2018-07-02
2209761203760934P160012LIFEPAK CR® Plus Defibrillator, LIFEPAK EXPRESS® Defibrillator, and CHARGE-PAK® Battery ChargerMKJ2017-12-21
2209761209220210K173553LUCAS 3 Chest Compression SystemDRM2018-02-08
2209761414256578K161768LUCAS 3 Chest Compression SystemDRM2016-11-09
2209761679063266K102972LIFEPAK 12MKJ2010-12-22
2209761969702614K090422LUCAS 2DRM2009-06-17
2209761569645854K052057LIFEPAK 500 AUTOMATED EXTERNAL DEFIBRILLATORMKJ2006-02-17

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
MKJ92018-12-21
DRM52018-02-08