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
1915434209
Device Listing 1915434209
Listing Summary
#
Listing key
1915434209
Premarket submission
K090834
Device
EPICARDIA 5000
Applicant
Medicomp, Inc.
Product code
DSI
Decision date
2009-05-15
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
285070
1033601
1033601
MEDICOMP, INC.
1
Y
2026-01-01
600 Atlantis Rd -- Melbourne FL US 32904