Emsi is one of 18967 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Emsi - FDA 510(k) Cleared Devices
Recent clearances: FLEX-MT +, GS 3000, EMSI GARMENT ELECTRODES
6
Total
6
Cleared
0
Denied
Emsi has 6 FDA 510(k) cleared medical devices. Based in Alexandria, US.
Historical record: 6 cleared submissions from 2008 to 2014. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Emsi Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.
FDA 510(k) Regulatory Record - Emsi
6 devices
Cleared
Oct 07, 2014
FLEX-MT +
Physical Medicine
225d
Cleared
Nov 23, 2010
GS 3000
Physical Medicine
111d
Cleared
Dec 04, 2009
EMSI GARMENT ELECTRODES
Neurology
248d
Cleared
May 08, 2009
FLEX-TENS
Neurology
51d
Cleared
Feb 05, 2009
TENS-EMS-14
Neurology
118d
Cleared
Mar 07, 2008
TENS/IF 14
Neurology
245d