Ars Enterprises, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ars Enterprises, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Ars Enterprises, Inc. has 4 FDA 510(k) cleared medical devices. Based in Anaheim, US.
Historical record: 4 cleared submissions from 1984 to 1985. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Ars Enterprises, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ars Enterprises, Inc.
4 devices
Cleared
Nov 01, 1985
ARS ENTERPRISES ETHYLENE OXIDE GAS STERILIZER
General Hospital
170d
Cleared
Sep 27, 1985
ARS ENTERPRISES NEW/REMFR'D GP STEAM STERILIZER 81
General Hospital
135d
Cleared
Sep 27, 1985
ARS ENTERPRISES PRE-VACUUM STEAM STERILIZER 85000
General Hospital
135d
Cleared
Jul 18, 1984
STEAM STERILIZER
General Hospital
449d