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
1868639674
Device Listing 1868639674
Listing Summary
#
Listing key
1868639674
Premarket submission
K963388
Device
VESSEL DILATOR
Applicant
Maxxim Medical
Product code
DRE
Decision date
1997-03-11
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
22447
1625425
1625425
ARGON MEDICAL DEVICES INC.
1
N
2026-01-01
1445 FLAT CREEK RD. ATHENS TX US 75751