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
1547153073
Device Listing 1547153073
Listing Summary
#
Listing key
1547153073
Premarket submission
K073326
Device
NRG TRANSSEPTAL NEEDLE
Applicant
Baylis Medical Co., Inc.
Product code
DXF
Decision date
2008-05-28
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
20121
9710452
3000157372
Rene van de Zande
1
N
2020-04-25
2500 Bee Cave Road Bldg 1, Suite 300 Austin TX US 78746