Amerasia Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Amerasia Corp. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Amerasia Corp. has 6 FDA 510(k) cleared medical devices. Based in Baldwin Park, US.
Historical record: 6 cleared submissions from 1995 to 1996. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Amerasia Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Amerasia Corp.
6 devices
Cleared
Mar 15, 1996
NIOMED SURGICAL CAPS
General & Plastic Surgery
80d
Cleared
Mar 06, 1996
NIOMED BARRIER GOWNS
General Hospital
142d
Cleared
Jan 23, 1996
NIOMED SURGICAL HOOD
General & Plastic Surgery
120d
Cleared
Jan 23, 1996
NIOMED BOUFFANT CAPS
General & Plastic Surgery
120d
Cleared
Oct 23, 1995
NIOMED SHOE COVERS
General Hospital
122d
Cleared
Oct 23, 1995
NIOMED NON-SKID SHOE COVERS
General Hospital
119d