Dayton Water Systems is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dayton Water Systems - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Dayton Water Systems has 3 FDA 510(k) cleared medical devices. Based in Dayton, US.
Historical record: 3 cleared submissions from 1995 to 2002. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Dayton Water Systems Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Dayton Water Systems
3 devices
Cleared
Aug 01, 2002
DAYTON WATER SYSTEMS ULTRAPURE WATER TREATMENT SYSTEMS FOR HEMODIALYSIS
Gastroenterology & Urology
94d
Cleared
Dec 31, 1998
ULTRAPURE WATER TREATMENT SYSTEM FOR HEMODIALYSIS
Gastroenterology & Urology
232d
Cleared
Aug 24, 1995
ASEPTECH PORTABLE RO+ SYSTEM
Gastroenterology & Urology
1071d