510(k) K891239

MOP CATHETER by Bivona Medical Technologies — Product Code KDL

K891239 is an FDA 510(k) premarket notification submitted by Bivona Medical Technologies for the device "MOP CATHETER". The FDA issued a decision of Substantially Equivalent on November 28, 1989. The device falls under product code KDL (Set, Perfusion, Kidney, Disposable), a Class II device regulated under 21 CFR 876.5880. Bivona Medical Technologies has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 28, 1989
Date Received
March 7, 1989
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Set, Perfusion, Kidney, Disposable
Device Class
Class II
Regulation Number
876.5880
Review Panel
GU
Submission Type