Dymedix, Inc. is one of 24282 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dymedix, Inc. - FDA 510(k) Cleared Devices
Recent clearances: DYMEDIX REUSABLE AIRFLOW/SNORE SENSOR, DYMEDIX REUSABLE RESPIRATORY EFFORT BELT SENSOR, MODEL 6015 AND DYMEDIX REUSABLE LIMB MOVEMENT SENSOR, MODEL 3100, CHIN ELECTRODE
4
Total
4
Cleared
0
Denied
Dymedix, Inc. has 4 FDA 510(k) cleared medical devices. Based in Stoughton, US.
Historical record: 4 cleared submissions from 2000 to 2004. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Dymedix, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Citech as regulatory consultant.
FDA 510(k) Regulatory Record - Dymedix, Inc.
4 devices
Cleared
May 05, 2004
DYMEDIX REUSABLE AIRFLOW/SNORE SENSOR
Anesthesiology
112d
Cleared
Apr 26, 2004
DYMEDIX REUSABLE RESPIRATORY EFFORT BELT SENSOR, MODEL 6015 AND DYMEDIX...
Anesthesiology
49d
Cleared
Apr 16, 2002
CHIN ELECTRODE
Neurology
63d
Cleared
May 11, 2000
RESPIRATORY BELT SENSOR, MODEL 6000S
Anesthesiology
42d