510(k) K171601

Ultraxx Nephrostomy Balloon Catheter by Cook Incorporated — Product Code LJE

K171601 is an FDA 510(k) premarket notification submitted by Cook Incorporated for the device "Ultraxx Nephrostomy Balloon Catheter". The FDA issued a decision of Substantially Equivalent on February 23, 2018. The device falls under product code LJE (Catheter, Nephrostomy), a Class U device. Cook Incorporated has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 23, 2018
Date Received
June 1, 2017
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Catheter, Nephrostomy
Device Class
Class U
Regulation Number
Review Panel
GU
Submission Type