Medi Tex, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medi Tex, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Medi Tex, Inc. has 4 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 4 cleared submissions from 1984 to 1992. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Medi Tex, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medi Tex, Inc.
4 devices
Cleared
Dec 04, 1992
LATEX EXAMINATION GLOVES
General Hospital
122d
Cleared
Apr 25, 1990
STERILE LATEX PATIENT EXAMINATION GLOVES
General Hospital
47d
Cleared
Mar 29, 1989
AMBIDERM(TM) PATIENT EXAMINATION GLOVE (LATEX)
General Hospital
16d
Cleared
Apr 13, 1984
INFUSION NEEDLE IIPN
General Hospital
39d