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
2027015851
Device Listing 2027015851
Listing Summary
#
Listing key
2027015851
Premarket submission
K112671
Device
STERILCONTAINER SYSTEM
Applicant
Aesculap, Ltd.
Product code
KCT
Decision date
2012-05-04
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
185419
3011824442
3011824442
Dan Eagar
1
N
2026-01-01
13320 Ballantyne Corp Pl Charlotte NC US 28277