# K960056: Usci Pro Flo XT,Soft Tip, and XT Soft Tip Angiographic

- Pathway: 510(k) (Traditional)
- Applicant: C.R. Bard, Inc.
- Decided: Oct 23, 1996 after 293 days
- Product code: DQO (Catheter, Intravascular, Diagnostic)
- Device class: 2
- Regulation: 21 CFR 870.1200
- 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 its predicate without a number.
- (no number) USCI® Positrol-II® Angiographic Catheter: named in the summary without a submission number
- (no number) Cordis® Super Torque Plus® Angiographic Catheter: named in the summary without a submission number

## Indications for use
The USCI® Pro-Flo, Pro-Flo with Soft Tip, Pro-Flo XT and Pro-Flo XT with Soft Tip are diagnostic intravascular catheters used to record intracardiac pressures, to sample blood, and to introduce substances into the heart and vessels.

Source page: https://510kreport.com/device/K960056
Methodology: https://510kreport.com/methodology