510(k) K980889

URESIL NEPHRO-URETERAL STENT by Uresil Corp. — Product Code LJE

K980889 is an FDA 510(k) premarket notification submitted by Uresil Corp. for the device "URESIL NEPHRO-URETERAL STENT". The FDA issued a decision of Substantially Equivalent on April 8, 1998. The device falls under product code LJE (Catheter, Nephrostomy), a Class U device. Uresil Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 8, 1998
Date Received
March 9, 1998
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