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
1164130950
Device Listing 1164130950
Listing Summary
#
Listing key
1164130950
Premarket submission
K150961
Device
EmbryoSlide Culture Dish
Applicant
Vitrolife A/S
Product code
MQK
Decision date
2015-12-04
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
140774
3009107689
3009107689
Erin Schardt
1
N
2026-01-01
3601 S Inca St Englewood CO US 80110