Rockwell Medical Technologies, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Rockwell Medical Technologies, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Rockwell Medical Technologies, Inc. has 5 FDA 510(k) cleared medical devices. Based in Wixom, US.
Historical record: 5 cleared submissions from 1999 to 2006. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Rockwell Medical Technologies, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Rockwell Medical Technologies, Inc.
5 devices
Cleared
Nov 17, 2006
ROCKWELL MEDICALTECHNOLOGIES, INC. CITRAPURE
Gastroenterology & Urology
93d
Cleared
Feb 28, 2003
ACIDIFIED COMPONENT CONCENTRATES FOR BICARBONATE DIALYSIS CONTAINING DI-ACETATE
Gastroenterology & Urology
88d
Cleared
Jan 03, 2003
BICARBONATE DIALYSATE CONCENTRATE MIXER, MODEL 50 GALLON & 100 GALLON
Gastroenterology & Urology
157d
Cleared
Dec 23, 2002
DRI-SATE DRY ACID CONCENTRATE FOR BICARBONATE DIALYSATE
Gastroenterology & Urology
147d
Cleared
Aug 05, 1999
DRI-SATE MIXER FOR PREPARATION OF ACIDIFIED DIALYSATE CONCENTRATE
Gastroenterology & Urology
294d