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
1295472081
Device Listing 1295472081
Listing Summary
#
Listing key
1295472081
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
212856
3015876
3015876
PHYSIO-CONTROL, INC.
1
Y
2026-01-01
11811 WILLOWS RD., N.E. Redmond WA US 98052