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
1539382977
Device Listing 1539382977
Listing Summary
#
Listing key
1539382977
Premarket submission
K141334
Device
REUSABLE GUIDE
Applicant
Koelis
Product code
ITX
Decision date
2014-07-11
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
121945
3008487708
3008487708
KOELIS
1
N
2027-01-01
22 Chemin Du Vieux Chene MEYLAN Isere FR 38240