Minntech Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Minntech Corp. - FDA 510(k) Cleared Devices
33
Total
33
Cleared
0
Denied
Minntech Corp. has 33 FDA 510(k) cleared medical devices. Based in Minneapolis, US.
Historical record: 33 cleared submissions from 1987 to 2012. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Minntech Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Minntech Corp.
33 devices
Cleared
Sep 27, 2012
RAPICIDE OPA-28
General Hospital
239d
Cleared
Apr 05, 2010
MEDIVATORS DSD EDGE ENDOSCOPE REPROCESSING SYSTEM
General Hospital
243d
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
Feb 01, 2002
ENGUARD CHC DUAL RESERVOIR CARDIOPLEGIA HEATER/COOLER
Cardiovascular
58d
Cleared
Jun 08, 2000
ENGUARD PHX CARDIOPLEGIA HEAT EXCHANGER
Cardiovascular
430d
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