510(k) K082536

COOK WIRE GUIDES by Cook Urological, Inc. — Product Code OCY

K082536 is an FDA 510(k) premarket notification submitted by Cook Urological, Inc. for the device "COOK WIRE GUIDES". The FDA issued a decision of Substantially Equivalent on October 27, 2008. The device falls under product code OCY (Endoscopic Guidewire, Gastroenterology-Urology), a Class II device regulated under 21 CFR 876.1500. Cook Urological, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 27, 2008
Date Received
September 2, 2008
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Endoscopic Guidewire, Gastroenterology-Urology
Device Class
Class II
Regulation Number
876.1500
Review Panel
GU
Submission Type

To provide access to gi or gu tract for the purpose of passing or exchanging other accessories.