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
1593023701
Device Listing 1593023701
Listing Summary
#
Listing key
1593023701
Premarket submission
K251185
Device
Recana Thrombectomy Catheter System (FG014. FG015, FG016, FG017, FG018, FG019, FG020)
Applicant
Intervene
Product code
QEW
Decision date
2025-10-22
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
344188
3030481118
3030481118
INTERVENE INC
1
N
2026-01-01
2684 Middlefield Rd Ste E Redwood City CA US 94063