Minntech Corp. - FDA 510(k) Cleared Devices
Recent clearances: RAPICIDE OPA-28, MEDIVATORS DSD EDGE ENDOSCOPE REPROCESSING SYSTEM, HF JUNIOR HEMOFILTER
33
Total
33
Cleared
0
Denied
FDA 510(k) Regulatory Record - Minntech Corp. Gastroenterology & Urology ✕
19 devices
Cleared
Aug 08, 2007
HF JUNIOR HEMOFILTER
Gastroenterology & Urology
91d
Cleared
Jan 31, 2006
HPH JUNIOR HIGH PERFORMANCE HEMOCONCENTRATOR
Gastroenterology & Urology
291d
Cleared
Apr 27, 2004
RENACLEAN SH DIALYZER CLEANING SYSTEM
Gastroenterology & Urology
174d
Cleared
Apr 04, 2000
RENAFLO II HF 2000 HEMOFILTER
Gastroenterology & Urology
90d
Cleared
Aug 30, 1999
RENACLEAR DIALYZER CLEANING SYSTEM
Gastroenterology & Urology
90d
Cleared
Mar 08, 1999
FIBERFLO HOLLOW FIBER CAPSULE WATER FILTERS
Gastroenterology & Urology
181d
Cleared
Nov 13, 1998
HEMOCOR HPH 700 HEMOCONCENTRATOR
Gastroenterology & Urology
71d
Cleared
May 12, 1998
HEMOCOR HPH MINI HEMOCONCENTRATOR
Gastroenterology & Urology
68d
Cleared
Oct 09, 1996
MINNTECH MINNIFILTER PLUS HEMOFILTER AND TUBING SET
Gastroenterology & Urology
89d
Cleared
Dec 15, 1995
FIBERFLO HOLLOW FIBER CARTRIDGE WATER FILTERS
Gastroenterology & Urology
88d
Cleared
Feb 28, 1995
RENAGUARD DIALYSATE FILTER
Gastroenterology & Urology
131d
Cleared
Jul 29, 1994
PRIMUS HOLLOW FIBER DIALYZER MOD. 1000, 1350, 2000
Gastroenterology & Urology
732d