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
1751213198
Device Listing 1751213198
Listing Summary
#
Listing key
1751213198
Premarket submission
K935994
Device
PW DOPPLER VASCULAR PROBES
Applicant
Koven Technology, Inc.
Product code
ITX
Decision date
1995-05-11
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