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
1747088737
Device Listing 1747088737
Listing Summary
#
Listing key
1747088737
Premarket submission
K063630
Device
ATRICURE ABLATION SYSTEM
Applicant
AtriCure, Inc.
Product code
GEI
Decision date
2007-01-26
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
192439
3011706110
3011706110
ATRICURE, INC.
1
N
2026-01-01
7555 Innovation Way Mason OH US 45040