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
1840862582
Device Listing 1840862582
Listing Summary
#
Listing key
1840862582
Premarket submission
K880860
Device
CORONARY OSTIUM OCCLUDER, CATALOG CODE 32015
Applicant
Dlp, Inc.
Product code
DQT
Decision date
1988-05-26
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
5792
2184009
1000116158
MEDTRONIC PERFUSION SYSTEMS
1
N
2026-01-01
7611 Northland Dr Minneapolis MN US 55428