Reprocessing Products Corp is one of 5250 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Reprocessing Products Corp - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Reprocessing Products Corp has 6 FDA 510(k) cleared medical devices. Based in Tucson, US.
Historical record: 6 cleared submissions from 1995 to 2013. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Reprocessing Products Corp Filter by specialty or product code using the sidebar.
Reprocessing Products Corp — FDA 510(k) Products and Clearance History
6 devices
Cleared
Mar 20, 2013
E-Z CHEK BLOOD LEAK TEST STRIPS
Gastroenterology & Urology
99d
Cleared
Jan 07, 2011
RPC E-Z CHEK 6.8-8.5 PH TEST STRIPS, MODEL K100-0117 AND E-Z CHEK 0-14 PH...
Gastroenterology & Urology
199d
Cleared
May 08, 2009
ULTRA LOW TOTAL CHLORINE, E-Z CHEK SENSITIVE TOTAL CHLORINE
Gastroenterology & Urology
87d
Cleared
Feb 10, 1999
POTENCY TEST STRIPS, INDICATOR TEST STRIPS
Gastroenterology & Urology
471d
Cleared
Dec 07, 1998
MICRO X RESIDUAL TEST STRIPS
Gastroenterology & Urology
406d
Cleared
Nov 30, 1995
PORT CAPS (PROTECTIVE CLOSURES FOE REPROCESSED HEMODIALYZERS
Gastroenterology & Urology
294d