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
1024609345
Device Listing 1024609345
Listing Summary
#
Listing key
1024609345
Premarket submission
P150026
Device
HEARTLIGHT ENDOSCOPIC ABLATION SYSTEM
Applicant
CARDIOFOCUS, INC.
Product code
OAE
Decision date
2016-04-01
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
42951
1222616
1000120916
PRECISION OPTICS CORP.
1
N
2026-01-01
22 E Broadway GARDNER MA US 01440