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
1871009888
Device Listing 1871009888
Listing Summary
#
Listing key
1871009888
Premarket submission
K183195
Device
VIVO
Applicant
Catheter Precision, Inc.
Product code
DQK
Decision date
2019-06-14
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
166519
3010728615
3010728615
Catheter Precision, Incorporated
1
N
2026-01-01
1670 Highway 160 West Suite 205 Fort Mill SC US 29708