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
1111111296
Device Listing 1111111296
Listing Summary
#
Listing key
1111111296
Premarket submission
K181919
Device
Patient Monitor
Applicant
Guangdong Biolight Meditech Co., Ltd.
Product code
MWI
Decision date
2019-04-05
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
135952
3009327812
3009327812
Proactive Medical Products
1
Y
2026-01-01
590 Franklin Ave Mount Vernon NY US 10550