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
1889187742
Device Listing 1889187742
Listing Summary
#
Listing key
1889187742
Premarket submission
K191088
Device
Checkme O2 Pulse Oximeter
Applicant
Shenzhen Viatom Technology Co., Ltd.
Product code
DQA
Decision date
2019-12-02
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
309026
3024722701
3024722701
WESPER INC. LIC
1
N
2026-01-01
44-02 11th St. Ste 610 Long Island City NY US 11101