510(k) K140482

MANDREL GUIDEWIRE by Lake Region Medical — Product Code OCY

K140482 is an FDA 510(k) premarket notification submitted by Lake Region Medical for the device "MANDREL GUIDEWIRE". The FDA issued a decision of Substantially Equivalent on April 8, 2014. The device falls under product code OCY (Endoscopic Guidewire, Gastroenterology-Urology), a Class II device regulated under 21 CFR 876.1500. Lake Region Medical has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 8, 2014
Date Received
February 26, 2014
Clearance Type
Special
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.