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
1098959298
Device Listing 1098959298
Listing Summary
#
Listing key
1098959298
Premarket submission
K082425
Device
TANDEMHEART TRANSSEPTAL CANNULA- EF 72
Applicant
Cardiacassist, Inc.
Product code
DWF
Decision date
2008-09-18
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
211009
1419629
1419629
Viant Medical, Inc.
1
N
2020-04-25
620 WATSON SW GR MI US 49504