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
1959636826
Device Listing 1959636826
Listing Summary
#
Listing key
1959636826
Premarket submission
K100662
Device
FEMVUE CORNUAL BALLOON CATHETER
Applicant
Femasys, Inc.
Product code
LKF
Decision date
2010-04-07
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
106734
3007800906
3007800906
FEMASYS INC.
1
N
2026-01-01
3950 Johns Creek Court Ste 100 Suwanee GA US 30024