Maytex Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Maytex Corp. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Maytex Corp. has 4 FDA 510(k) cleared medical devices. Based in Hayward, US.
Historical record: 4 cleared submissions from 1989 to 1994. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Maytex Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Maytex Corp.
4 devices
Cleared
Aug 01, 1994
MAYTEX LATEX EXAMINATION GLOVES, POWDERED
General Hospital
272d
Cleared
Aug 01, 1994
MAYTEX POWDER-FREE LATEX EXAMINATION GLOVES
General Hospital
272d
Cleared
May 31, 1989
MAYTEX NON-STERILE LATEX EXAM GLOVES
General Hospital
58d
Cleared
May 31, 1989
MAYTEX LATEX EXAMINATION GLOVES
General Hospital
56d