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
2048595869
Device Listing 2048595869
Listing Summary
#
Listing key
2048595869
Premarket submission
K941461
Device
DYNATRON 850
Applicant
Dynatronics Research Corp.
Product code
LIH
Decision date
1995-09-01
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
69016
1719362
1719362
DYNATRONICS CORP.
1
Y
2020-04-25
7030 PARK CENTRE DR. Salt Lake City UT US 84121