Skip to content
FDA.report
Public FDA data
NDC
RxNorm
DailyMed
Applications
GUDID
GMDN
PMA
PMN
MAUDE
Recalls
Search FDA.report
Search
Home
Company-Registration
1855522004
Device Listing 1855522004
Listing Summary
#
Listing key
1855522004
Premarket submission
K052057
Device
LIFEPAK 500 AUTOMATED EXTERNAL DEFIBRILLATOR
Applicant
Medtronic Emergency Response Systems, Inc.
Product code
MKJ
Decision date
2006-02-17
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
185359
3011823740
3011823740
Greatbatch Medical S. de R.L. de C.V.
1
N
2026-01-01
Calle 5 Norte No. 511 Ciudad Industrial Tijuana Baja California MX 22444