FDA.reportPublic FDA data

Device Listing 1231801124

Listing Summary#

Listing key
1231801124
Premarket submission
K130725
Device
MODIFIED ARGYLE POLYURETHANE UMBILICAL VESSEL CATHETER 2.5FR, 3.5FR, 5 FR.
Applicant
Covidien Lp, Formerly Registered AS Kendall
Product code
FOS
Decision date
2013-04-17