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
1417659819
Device Listing 1417659819
Listing Summary
#
Listing key
1417659819
Premarket submission
K924646
Device
OVER THE GUIDEWIRE DILATATION SYSTEM
Applicant
Medovations, Inc.
Product code
KNQ
Decision date
1994-12-05
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
6100
2183446
2183446
DIVERSATEK HEALTHCARE INC
1
Y
2026-01-01
102 EAST KEEFE AVE. Milwaukee WI US 53212