American Health Products, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
American Health Products, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
American Health Products, Inc. has 5 FDA 510(k) cleared medical devices. Based in Orange, US.
Historical record: 5 cleared submissions from 1988 to 1998. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by American Health Products, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - American Health Products, Inc.
5 devices
Cleared
Jan 29, 1998
SURGEON'S GLOVES
General Hospital
71d
Cleared
Dec 15, 1992
PATIENT EXAM GLOVES (POWDER FREE)
General Hospital
131d
Cleared
May 11, 1989
PATIENT EXAM GLOVES (MFG. AMERICAN RUBBER PRODUCT)
General Hospital
35d
Cleared
Apr 28, 1989
PATIENT EXAM GLOVES (MFG. MULTI-COM SDN BHD)
General Hospital
22d
Cleared
Jun 15, 1988
MONITRON SYSTEM
Cardiovascular
246d