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
1222016691
Device Listing 1222016691
Listing Summary
#
Listing key
1222016691
Premarket submission
K061571
Device
ASTRA 300
Applicant
Sdi Diagnostics, Inc.
Product code
BZG
Decision date
2007-01-31
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
30278
1220253
1220253
SDI DIAGNOSTICS, INC.
1
N
2026-01-01
10 Hampden Dr South Easton MA US 02375