Pure Water, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pure Water, Inc. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Pure Water, Inc. has 3 FDA 510(k) cleared medical devices. Based in Anderson, US.
Historical record: 3 cleared submissions from 2000 to 2000. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Pure Water, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Pure Water, Inc.
3 devices
Cleared
Apr 10, 2000
PURE WATER, INC.'S BICARB MIX, STORAGE AND DISTRIBUTION SYSTEM
Gastroenterology & Urology
193d
Cleared
Jan 24, 2000
PURE WATER, INC.'S WATER PURIFICATION SYSTEMS
Gastroenterology & Urology
158d
Cleared
Jan 24, 2000
PURE WATER INC'S ACIDIFIED STORAGE AND DISTRIBUTION SYSTEM WITH OPTIONAL...
Gastroenterology & Urology
133d