Ameco Medical Industries is one of 15081 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ameco Medical Industries - FDA 510(k) Cleared Devices
Recent clearances: Amecath Peripheral inserted Central Venous Catheter Sets, AMECO SHEATH INTRODUCER, AMECATH DUAL LUMEN IMPLANTED HEMODIALYSIS CATHETER
6
Total
5
Cleared
0
Denied
Ameco Medical Industries has 5 FDA 510(k) cleared medical devices. Based in Mason, US.
Historical record: 5 cleared submissions from 2011 to 2016. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Ameco Medical Industries Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Licensale, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Ameco Medical Industries
6 devices
Cleared
Feb 05, 2016
Amecath Peripheral inserted Central Venous Catheter Sets
General Hospital
130d
Cleared
Aug 15, 2013
AMECO SHEATH INTRODUCER
Cardiovascular
114d
Cleared
Jul 26, 2013
AMECATH DUAL LUMEN IMPLANTED HEMODIALYSIS CATHETER
Gastroenterology & Urology
36d
Cleared
Apr 02, 2013
AMECATH DUAL LUMEN HEMODIALYSIS CATHETER
Gastroenterology & Urology
103d
Cleared
Dec 21, 2011
AMECATH CVC AND AMECATH PRESSURE CVC SHORT TERM SINGLE AND MULTI-LUMEN...
General Hospital
274d
Cleared
Dec 16, 2011
AMECATH AND AMECATH UNIQATH SOFT SHORT TERM DUAL HEMODIALYSIS CATHETERIZATION...
Gastroenterology & Urology
269d