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
2040213356
Device Listing 2040213356
Listing Summary
#
Listing key
2040213356
Premarket submission
K062725
Device
MAXIFLEX-SEMI FLEX SCOPE
Applicant
Technology Delivery Systems, Inc.
Product code
FGB
Decision date
2006-09-29
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
72918
3006812215
3006812215
MAXIFLEX, LLC
1
N
2020-04-25
512 Verret St New Orleans LA US 70114