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
2044431334
Device Listing 2044431334
Listing Summary
#
Listing key
2044431334
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
66655
3005875675
3005875675
GYNESONICS, INC.
1
N
2020-04-25
600 Chesapeake Drive REDWOOD CITY CA US 94063