# P890048: Usci Probe Iii Balloon-on-a-Wire Dilatation System

- Pathway: PMA
- Applicant: Usci, Div. C.R. Bard, Inc.
- Decided: Apr 17, 1991 after 596 days
- Product code: LOX (Catheters, Transluminal Coronary Angioplasty, Percutaneous)
- Device class: 2
- Regulation: 21 CFR 870.5100
- 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. PMA decisions do not claim a predicate device.

Source page: https://510kreport.com/device/P890048
Methodology: https://510kreport.com/methodology