# K854511: Elecath Percutaneous Left Atrial Cannulation Set

- Pathway: 510(k) (Traditional)
- Applicant: Electro-Catheter Corp.
- Decided: Feb 10, 1986 after 90 days
- Product code: DQX (Wire, Guide, Catheter)
- Device class: 2
- Regulation: 21 CFR 870.1330
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
11 later devices descend from it; 1 cites it directly.
2 of 12 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K030398: Cardiacassist Transseptal Cannula Set, Model 5132-6221 (2003), 10 descendants of its own
- K052570: Tandemheart Transseptal Cannula Set-EF, Model 5140-6221 (2006), 9 descendants of its own
- K063723: Impella Recover LP 2.5 Percutaneous Cardiac Support System (2008), 7 descendants of its own
- K083111: Impella 5.0 Catheter Family (2009), 3 descendants of its own
- K102726: Cardiohelp System (2011), 2 descendants of its own

Source page: https://510kreport.com/device/K854511
Methodology: https://510kreport.com/methodology