510(k) K081708

TAXI ENDOSCOPIC GUIDEWIRE by Lake Region Mfg., Inc. — Product Code OCY

K081708 is an FDA 510(k) premarket notification submitted by Lake Region Mfg., Inc. for the device "TAXI ENDOSCOPIC GUIDEWIRE". The FDA issued a decision of Substantially Equivalent on August 26, 2008. The device falls under product code OCY (Endoscopic Guidewire, Gastroenterology-Urology), a Class II device regulated under 21 CFR 876.1500. Lake Region Mfg., Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 26, 2008
Date Received
June 17, 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.