510(k) K123439

NEO ERCP GUIDEWIRE by Neometrics, Inc. — Product Code OCY

K123439 is an FDA 510(k) premarket notification submitted by Neometrics, Inc. for the device "NEO ERCP GUIDEWIRE". The FDA issued a decision of Substantially Equivalent on January 3, 2013. The device falls under product code OCY (Endoscopic Guidewire, Gastroenterology-Urology), a Class II device regulated under 21 CFR 876.1500. Neometrics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 3, 2013
Date Received
November 8, 2012
Clearance Type
Traditional
Expedited Review
No
Third Party Review
Yes

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.