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
1822086584
Device Listing 1822086584
Listing Summary
#
Listing key
1822086584
Premarket submission
K221175
Device
Multi-Lancet Device 2, ReliOn Premier Lancing Device
Applicant
Arkray, Inc.
Product code
QRL
Decision date
2022-10-17
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
204146
3013472743
3013472743
Yosuke Yamamoto
1
N
2026-01-01
8260 NW 27th Street, Suite 403 Miami FL US 33122