FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

ALL SILICONE FOLEY CATHETER

K Number: K896053 · Decision Feb 12, 1990
Classifications
1
FEI Numbers
114
Registration Numbers
114
Same Product Code
237
Applicant Total
13
Review Days
117

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Basic Information

Device Name
ALL SILICONE FOLEY CATHETER
K Number
K896053
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5130
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Rochester Medical Corp.
Date Received
October 18, 1989
Decision Date
February 12, 1990
Product Code
KOD
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KOD Catheter, Urological

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KOD), ordered by most recent decision date.

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Other Clearances by Rochester Medical Corp.

K Number Device Name
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
Search all 13 clearances from Rochester Medical Corp. →