Alatech Healthcare, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Alatech Healthcare, LLC - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Alatech Healthcare, LLC has 4 FDA 510(k) cleared medical devices. Based in Eufaula, US.
Historical record: 4 cleared submissions from 1999 to 2009. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Alatech Healthcare, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Alatech Healthcare, LLC
4 devices
Cleared
Jul 22, 2009
ALATECH POWDER FREE LATEX EXAMINATION GLOVE
General Hospital
216d
Cleared
May 01, 2009
ALATECH CHAMPION VYTEX LUBRICATED MALE LATEX CONDOM
Obstetrics & Gynecology
241d
Cleared
Aug 07, 2008
ALATECH POWDERED LATEX PATIENT EXAMINATION GLOVE
General Hospital
156d
Cleared
Dec 20, 1999
ALATECH LATEX CONDOM
Obstetrics & Gynecology
34d