510(k) K863302

MODIFIED FOLEY CATHETER by Sheridan Catheter Corp. — Product Code KOD

K863302 is an FDA 510(k) premarket notification submitted by Sheridan Catheter Corp. for the device "MODIFIED FOLEY CATHETER". The FDA issued a decision of Substantially Equivalent on October 3, 1986. The device falls under product code KOD (Catheter, Urological), a Class II device regulated under 21 CFR 876.5130. Sheridan Catheter Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 3, 1986
Date Received
August 25, 1986
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Catheter, Urological
Device Class
Class II
Regulation Number
876.5130
Review Panel
GU
Submission Type