510(k) K891239
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