# K960920: Clinix MP

- Pathway: 510(k) (Traditional)
- Applicant: Philips Medical Systems (Cleveland), Inc.
- Decided: May 20, 1996 after 75 days
- Product code: OWB (Interventional Fluoroscopic X-Ray System)
- Device class: 2
- Regulation: 21 CFR 892.1650
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names no predicate by number.

## Indications for use
Routine Radiolgraphic/Fluoroscopic examinations of the entire hut.n.an anatomy, gastrointestinal tract, full vascular/interventional capabilities, and organ examinations.

Source page: https://510kreport.com/device/K960920
Methodology: https://510kreport.com/methodology