510(k) K942688

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

K942688 is an FDA 510(k) premarket notification submitted by Uresil Corp. for the device "NEPHRO-URETERAL STENT". The FDA issued a decision of Substantially Equivalent on June 6, 1995. 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
June 6, 1995
Date Received
June 7, 1994
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