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
1476646175
Device Listing 1476646175
Listing Summary
#
Listing key
1476646175
Premarket submission
K081104
Device
AESKULISA ANA HEP-2, REF 30-7115US
Applicant
Aesku Diagnostics
Product code
LKJ
Decision date
2008-05-02
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
193625
1000124057
1000124057
GRIFOLS DIAGNOSTIC SOLUTIONS INC.
1
Y
2026-01-01
4560 HORTON ST Emeryville CA US 94608