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
1719521954
Device Listing 1719521954
Listing Summary
#
Listing key
1719521954
Premarket submission
K960070
Device
NUMED ATRIOSEPTOSTOMY CATHETER
Applicant
NuMED, Inc.
Product code
DQO
Decision date
1996-04-02
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
2004
1318694
1318694
NUMED, INC.
1
Y
2026-01-01
2880 MAIN ST. Hopkinton NY US 12965