Ash Medical Systems, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ash Medical Systems, Inc. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Ash Medical Systems, Inc. has 3 FDA 510(k) cleared medical devices. Based in West Lafayette, US.
Historical record: 3 cleared submissions from 1986 to 1988. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Ash Medical Systems, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ash Medical Systems, Inc.
3 devices
Cleared
Apr 08, 1988
MODIFIED BIOLOGIC 1000 HEMODIAL. & HD-1000 DIS CAR
Gastroenterology & Urology
178d
Cleared
Feb 25, 1987
MODIFIED BIO. HEMODIALYSIS & HD-1000 DISP. CART.
Gastroenterology & Urology
29d
Cleared
Dec 11, 1986
BIOLOGIC 1000 HEMODIALYSIS MACH/HD-1000 DISP CARTR
Gastroenterology & Urology
48d