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
1574959070
Device Listing 1574959070
Listing Summary
#
Listing key
1574959070
Premarket submission
K861496
Device
STOCKERT-SHILEY VENOUS CATH & AORTIC ARCH CANNULA
Applicant
Shiley, Inc.
Product code
DWF
Decision date
1986-05-27
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
176608
3006948478
3006948478
STERIS SPA
1
N
2020-04-25
via A. Piva Poggio Rusco Mantova IT 46025