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
1356141288
Device Listing 1356141288
Listing Summary
#
Listing key
1356141288
Premarket submission
K093233
Device
D3 FASTPOINT L-DFA RSV/MVP IDENTIFICATION KIT
Applicant
Diagnostic Hybrids, Inc.
Product code
OMG
Decision date
2009-12-04
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
13086
1528450
1000122536
QUIDEL CORPORATION
1
N
2020-04-25
2005 East State Street, Suite 100 ATHENS OH US 45701