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
1622744234
Device Listing 1622744234
Listing Summary
#
Listing key
1622744234
Premarket submission
K142692
Device
Occlusion Balloon Catheter
Applicant
Embolx, Inc.
Product code
MJN
Decision date
2015-05-31
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
184524
3011660785
3011660785
EMBOLX INC.
1
N
2026-01-01
530 Lakeside Dr Ste 150 Sunnyvale CA US 94085