Mexpo Intl., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Mexpo Intl., Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Mexpo Intl., Inc. has 4 FDA 510(k) cleared medical devices. Based in Hayward,, US.
Historical record: 4 cleared submissions from 1998 to 1999. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Mexpo Intl., Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Mexpo Intl., Inc.
4 devices
Cleared
Aug 17, 1999
BLOSSOM POWDER FREE LATEX EXAMINATION GLOVES WITH PROTEIN CONTENT LABELING...
General Hospital
35d
Cleared
Mar 29, 1999
POWDERED LATEX EXAMINATION GLOVES WITH PROTEIN CONTENT LABELING CLAIM (100...
General Hospital
67d
Cleared
Jan 13, 1999
BLOSSOM POWDERED LATEX EXAMINATION GLOVES
General Hospital
62d
Cleared
Feb 24, 1998
LOW PROTEIN POWDER FREE LATEX EXAMINATION GLOVES
General Hospital
64d