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
1012763084
Device Listing 1012763084
Listing Summary
#
Listing key
1012763084
Premarket submission
K120674
Device
MAHURKAR ELITE ACUTE DUAL LUMEN CATHETER, ELITE ACUTE TRIPLE LUMEN CATHETER
Applicant
Covidien
Product code
MPB
Decision date
2012-04-04
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
329409
3030574705
3030574705
MOZARC MEDICAL US LLC
1
Y
2026-01-01
15 Hampshire Street Mansfield MA US 02048