Ameriwater is one of 5098 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ameriwater - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
Ameriwater has 11 FDA 510(k) cleared gastroenterology & urology devices. Based in Dayton, US.
Historical record: 11 cleared submissions from 2000 to 2014.
Browse the complete list of FDA 510(k) cleared gastroenterology & urology devices from this manufacturer. Filter by specialty or product code using the sidebar.
Ameriwater — FDA 510(k) Products and Clearance History
11 devices
Cleared
Dec 10, 2014
AMERIWATER OZONE DISINFECTION SYSTEM
Gastroenterology & Urology
212d
Cleared
Dec 01, 2014
AmeriWater Heatsan, 3-phase, 208v, 60hz, AmeriWater Heatsan, 3-phase, 460V,...
Gastroenterology & Urology
105d
Cleared
Apr 16, 2014
AMERIWATER CENTURION 1500+ REVERSE OSMOSIS SYSTEM WITH HEAT SANITIZATION
Gastroenterology & Urology
125d
Cleared
Nov 13, 2013
MEDIQA SINGLE PASS REVERSE OSMOSIS SYSTEM WITH HEAT SANITIZATION, MEDIQA...
Gastroenterology & Urology
141d
Cleared
Sep 20, 2013
MROZ REVERSE OSMOSIS SYSTEM
Gastroenterology & Urology
109d
Cleared
Sep 17, 2012
AMERIWATER ALARM PANEL - BASE MODEL AND REMOTE, BASE MODEL & REMOTE WITH...
Gastroenterology & Urology
166d
Cleared
Oct 05, 2011
AMERIWATER MRO PORTABLE REVERSE OSMOSIS SYSTEM - SINGLE PATIENT, 1 TO 3 STATION
Gastroenterology & Urology
106d
Cleared
Jan 06, 2006
AMERIWATER SOLUTION MIX AND DISTRIBUTION SYSTEM FOR HEMODIALYSIS
Gastroenterology & Urology
259d
Cleared
Aug 14, 2003
MODIFICATION TO AMERIWATER PURIFICATION SYSTEM FOR HEMODIALYSIS
Gastroenterology & Urology
458d
Cleared
Apr 07, 2003
PORTABLE RO+ MODEL MROS09
Gastroenterology & Urology
90d
Cleared
Apr 14, 2000
AMERIWATER PURIFICATION SYSTEM FOR HEMODIALYSIS
Gastroenterology & Urology
350d