510(k) K830226

SURGITEK PERCUTANEOUS NEPHROSTOMY CATH by Medical Engineering Corp. — Product Code LJE

K830226 is an FDA 510(k) premarket notification submitted by Medical Engineering Corp. for the device "SURGITEK PERCUTANEOUS NEPHROSTOMY CATH". The FDA issued a decision of Substantially Equivalent on February 9, 1983. The device falls under product code LJE (Catheter, Nephrostomy), a Class U device. Medical Engineering Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 9, 1983
Date Received
January 24, 1983
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