510(k) K980193

MANAN GENERAL UTILITY DRAINAGE CATHETER by Medical Device Technologies, Inc. — Product Code LJE

K980193 is an FDA 510(k) premarket notification submitted by Medical Device Technologies, Inc. for the device "MANAN GENERAL UTILITY DRAINAGE CATHETER". The FDA issued a decision of Substantially Equivalent on May 27, 1998. The device falls under product code LJE (Catheter, Nephrostomy), a Class U device. Medical Device Technologies, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 27, 1998
Date Received
January 20, 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