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
2052421642
Device Listing 2052421642
Listing Summary
#
Listing key
2052421642
Premarket submission
K173903
Device
Granada Medium
Applicant
Hardy Diagnostics
Product code
PQZ
Decision date
2018-03-22
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
34263
2022807
2022807
HARDY DIAGNOSTICS
1
Y
2026-01-01
1430 WEST MCCOY LN. Orcutt CA US 93455
140824
3009547954
3009547954
Hardy Diagnostics
1
N
2026-01-01
429 S Pioneer Blvd Springboro OH US 45066