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
1529278061
Device Listing 1529278061
Listing Summary
#
Listing key
1529278061
Premarket submission
K200941
Device
Rapid LVO
Applicant
Ischemaview, Inc.
Product code
QAS
Decision date
2020-07-09
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
175771
3011205675
3014269683
ISCHEMAVIEW, INC.
1
N
2026-01-01
1120 Washington Ave Ste 200, #108 Golden CO US 80401