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
2027119623
Device Listing 2027119623
Listing Summary
#
Listing key
2027119623
Premarket submission
K010864
Device
ANALYST PANELS + ANALYTICAL TEST ROTOR
Applicant
Hemagen Diagnostics, Inc.
Product code
KHS
Decision date
2001-05-21
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
1597
1181055
1181055
HEMAGEN DIAGNOSTICS, INC.
1
N
2026-01-01
2900 LOCH RAVEN RD Baltimore MD US 21218