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
1116748538
Device Listing 1116748538
Listing Summary
#
Listing key
1116748538
Premarket submission
K161916
Device
TelePatch Cardiac Monitor
Applicant
Medicomp, Inc.
Product code
DRG
Decision date
2016-12-21
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