# K960098: Rmi Internal Mammary Artery Cannula

- Pathway: 510(k) (Traditional)
- Applicant: Research Medical, Inc.
- Decided: Mar 26, 1996 after 75 days
- Product code: DQR (Cannula, Catheter)
- Device class: 2
- Regulation: 21 CFR 870.1300
- 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) DLP I.M.A. Cannula, Code #31001: named in the summary without a submission number

Source page: https://510kreport.com/device/K960098
Methodology: https://510kreport.com/methodology