510(k) K933110

OLYMPUS GUIDE WIRE by Olympus Corp. — Product Code OCY

K933110 is an FDA 510(k) premarket notification submitted by Olympus Corp. for the device "OLYMPUS GUIDE WIRE". The FDA issued a decision of Substantially Equivalent on November 4, 1993. The device falls under product code OCY (Endoscopic Guidewire, Gastroenterology-Urology), a Class II device regulated under 21 CFR 876.1500. Olympus Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 4, 1993
Date Received
June 25, 1993
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.