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
1067522037
Device Listing 1067522037
Listing Summary
#
Listing key
1067522037
Premarket submission
K991903
Device
EXCEL PHOTIC STIMULATOR, MODEL (XLPS-1)
Applicant
Excel Tech. , Ltd.
Product code
GWE
Decision date
1999-08-04
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
79228
9612330
3002809369
Courtney Walton
1
N
2026-01-01
3610 County Road 101 S Wayzata MN US 55391