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
1938297651
Device Listing 1938297651
Listing Summary
#
Listing key
1938297651
Premarket submission
K173703
Device
Sonata Sonography-Guided Transcervical Fibroid Ablation System
Applicant
Gynesonics, Inc.
Product code
KNF
Decision date
2018-08-15
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
33706
1930027
1930027
KATECHO LLC
1
N
2026-01-01
4020 GANNETT AVENUE. DES MOINES IA US 50321