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
1220132942
Device Listing 1220132942
Listing Summary
#
Listing key
1220132942
Premarket submission
K191853
Device
Dual-Safety Pen Needle
Applicant
Promisemed Hangzhou Meditech Co., Ltd.
Product code
FMI
Decision date
2019-09-05
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
348205
3038356900
3038356900
Carson Harvey
1
N
2026-01-01
311 S Wacker Dr Ste 4100 Chicago IL US 60606
349509
3044026004
3044026004
Carson Harvey
1
N
2026-01-01
311 S Wacker Dr Ste 4100 Chicago IL US 60606