Rochester Medical Corp.
Rochester Medical Corp. holds FDA 510(k) medical device clearances, first cleared 1990, most recent 2013.
Top product codes for Rochester Medical Corp.
Recent clearances by Rochester Medical Corp.
- K122785 — HYDROSIL; MAGIC; PERSONAL CATHETER
- K033477 — HYDROPHILIC-ANTIBACTERIAL INTERMITTENT CATHETER, INTERMITTENT CATHETER CLOSED SYSTEM KIT
- K001143 — RELEASE NF ANTIBACTERIAL FOLEY CATHETER, ANTIBACTERIAL PERSONAL CATHETER
- K000723 — HYDROPHILIC SILICONE FOLEY CATHETER AND PERSONAL CATHETER (HYDROPHILIC AND NON-HYDROPHILIC)
- K981612 — ALL SILICONE FOLEY CATHETER, TWO-WAY FOLEY CATHETER, THREE-WAY FOLEY CATHETER, TWO-WAY RADIOPAQUE FOLEY CATHETER
- K971627 — SILICONE ANTIBACTERIAL FOLEY CATHETER
- K970704 — PERSONAL CATHETER
- K952082 — ROCHESTER MEDICAL CORPORATION SILICONE MALE EXTERNAL CATHETER
- K941692 — FEMALE LENGTH ALL SILICONE UROLOGICAL CATHETER
- K943851 — ALL SILICONE INTERMITTENT CATHETER
- K923136 — MALE EXTERNAL CATHETER
- K905042 — COMFORT SLEEVED ALL SILICONE FOLEY CATHETER
- K896053 — ALL SILICONE FOLEY CATHETER
Data sourced from openFDA. This site is unofficial and independent of the FDA.