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
1730610123
Device Listing 1730610123
Listing Summary
#
Listing key
1730610123
Premarket submission
K915550
Device
MINI DOPPLER II ULTRASOUND BLOOD FLOW DETECTOR
Applicant
Koven and Assoc., Inc.
Product code
DPW
Decision date
1992-12-10
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
33822
1937397
1937397
KOVEN TECHNOLOGY, INC.
1
Y
2026-01-01
477 N Lindbergh Blvd SUITE 220 Saint Louis MO US 63141