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
1391322783
Device Listing 1391322783
Listing Summary
#
Listing key
1391322783
Premarket submission
K093447
Device
CARRIGEN
Applicant
Etex Corp.
Product code
MQV
Decision date
2010-02-18
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
72778
1225112
3000206397
ETEX Corporation
1
N
2026-01-01
55 Messina Dr Braintree MA US 02184