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
1317907784
Device Listing 1317907784
Listing Summary
#
Listing key
1317907784
Premarket submission
K180517
Device
CorPath GRX System
Applicant
Corindus, Inc.
Product code
DXX
Decision date
2018-03-29
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
138471
3007822508
3007822508
CORINDUS, INC.
1
N
2020-04-25
309 Waverley Oaks Rd Ste 105 Waltham MA US 02452