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
1315449841
Device Listing 1315449841
Listing Summary
#
Listing key
1315449841
Premarket submission
K221541
Device
LimFlow ARC
Applicant
LimFlow, Inc.
Product code
PDU
Decision date
2022-08-31
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
338183
3023527320
3023527320
LimFlow Inc.
1
N
2026-01-01
6001 Oak Canyon Suite 100 Irvine CA US 92618