510(k) K952887

NOPROFILE OLBERT CATHETER SYSTEM BALLOON DILATATION CATHETER by Meadox Medicals, Div. Boston Scientific Corp. — Product Code LJE

K952887 is an FDA 510(k) premarket notification submitted by Meadox Medicals, Div. Boston Scientific Corp. for the device "NOPROFILE OLBERT CATHETER SYSTEM BALLOON DILATATION CATHETER". The FDA issued a decision of Substantially Equivalent on August 18, 1995. The device falls under product code LJE (Catheter, Nephrostomy), a Class U device. Meadox Medicals, Div. Boston Scientific Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 18, 1995
Date Received
June 23, 1995
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