510(k) K123439
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.