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
1954826965
Device Listing 1954826965
Listing Summary
#
Listing key
1954826965
Premarket submission
K200094
Device
speX LP Support Catheter
Applicant
Reflow Medical
Product code
DQY
Decision date
2020-03-18
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
124285
3008789872
3008789872
REFLOW MEDICAL, INC
1
N
2026-01-01
208 Avenida Fabricante Suite 100 San Clemente CA US 92672
316217
3027058844
3027058844
Reflow Medical
1
N
2026-01-01
20532 Crescent Bay Dr. Suite 100 Lake Forest CA US 92630