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
1566222629
Device Listing 1566222629
Listing Summary
#
Listing key
1566222629
Premarket submission
K232588
Device
Aluna 2
Applicant
Knox Medical Diagnostics
Product code
BZH
Decision date
2024-11-25
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
242952
3016670256
3016670256
Mani Shanmugham
1
N
2026-01-01
14 Penn Plaza Floor 9 225 West 34th Street New York City NY US 10122