FDA.reportPublic FDA data

DYMEDIX DIAGNOSTICS INC

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30093517733009351773DYMEDIX DIAGNOSTICS INC1N2026-01-015985 Rice Creek Pkwy Ste 102 Shoreview MN US 55126

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
1368941003659232K990321ALPHAMED GEMINI SENSOR, SNORING SENSORMNR1999-06-01
1368941071794010K192564Disposable Gold Cup EEG ElectrodesGXY2020-01-21
1368941210586501K040605DYMEDIX REUSABLE RESPIRATORY EFFORT BELT SENSOR, MODEL 6015 AND DYMEDIX REUSABLE LIMB MOVEMENT SENSOR, MODEL 3100BZQ2004-04-26
1368941455781802K040069DYMEDIX REUSABLE AIRFLOW/SNORE SENSORMNR2004-05-05
1368941921323640K020468CHIN ELECTRODEGXY2002-04-16
1368942067792716K001030RESPIRATORY BELT SENSOR, MODEL 6000S; LIMB MOVEMENT SENSOR, MODEL 3000SBZQ2000-05-11
1368941932886258

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
GXY22020-01-21
MNR22004-05-05
BZQ22004-04-26