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
1024487965
Device Listing 1024487965
Listing Summary
#
Listing key
1024487965
Premarket submission
K162946
Device
8ch Knee-Foot SPEEDER
Applicant
Quality Electrodynamics, LLC
Product code
MOS
Decision date
2017-01-06
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
195378
3007350713
3007350713
QUALITY ELECTRODYNAMICS
1
N
2026-01-01
6655 Beta Drive Suite 100 Mayfield Village OH US 44143