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
1373188271
Device Listing 1373188271
Listing Summary
#
Listing key
1373188271
Premarket submission
K925081
Device
SURFAS
Applicant
D.O. Weaver and Co.
Product code
ITX
Decision date
1993-09-28
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
74087
1718791
1718791
D. O. WEAVER AND COMPANY
1
N
2026-01-01
565 NUCLA WAY, UNIT B Aurora CO US 80011