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
1379983299
Device Listing 1379983299
Listing Summary
#
Listing key
1379983299
Premarket submission
K932184
Device
STERILE LEMAITRE GLOW 'N TELL TAPE
Applicant
Vascutech, Inc.
Product code
KFX
Decision date
1993-07-22
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
30415
1220948
1220948
LEMAITRE VASCULAR, INC.
1
N
2026-01-01
63 SECOND AVENUE BURLINGTON MA US 01803