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
1639720533
Device Listing 1639720533
Listing Summary
#
Listing key
1639720533
Premarket submission
K955132
Device
HEARTPORT ENDOAORTIC CLAMP
Applicant
Heartport, Inc.
Product code
DXC
Decision date
1996-06-07
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
335141
3031571797
3031571797
ENABLECV, LLC
1
N
2026-01-01
6967 S River Gate Dr. Ste 104 Midvale UT US 84047