Minntech Corp. - FDA 510(k) Cleared Devices
33
Total
33
Cleared
0
Denied
FDA 510(k) Regulatory Record - Minntech Corp. General Hospital ✕
6 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
Oct 01, 1997
PERACT 20 LIQUID STERILANT
General Hospital
604d
Cleared
Jun 26, 1995
RENALIN COLD STERILANT
General Hospital
459d
Cleared
Feb 07, 1994
ENDPOINT 500 PERACETIC ACID TEST INDICATORS
General Hospital
294d
Cleared
Jan 09, 1989
RENALIN COLD STERILANT
General Hospital
202d