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
1314325529
Device Listing 1314325529
Listing Summary
#
Listing key
1314325529
Premarket submission
K173123
Device
Pulse Oximeter
Applicant
Shenzhen Imdk Medical Technology Co., Ltd.
Product code
DQA
Decision date
2018-08-13
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
199809
3012777736
3012777736
EMSRUN GROUP
1
N
2026-01-01
8-7 Huide Road, Huishan Area Wuxi Jiangsu CN 214000