# K952984: Map Multitrack Angiographic Catheter (4F)

- Pathway: 510(k) (Traditional)
- Applicant: Map Medical Equipment, Inc.
- Decided: Jan 29, 1996 after 215 days
- Product code: DQO (Catheter, Intravascular, Diagnostic)
- Device class: 2
- Regulation: 21 CFR 870.1200
- Recalls of this device: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 1 cites it directly.
0 of 3 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
- K040830: Pta, PTV, Atrioseptostomy, Angiographic, Sizing Catheters (2004), 1 descendant of its own
- K153069: Edwards Balloon Catheter (2016), 0 descendants of its own

## Recalls of this device
- Oct 17, 2018 · Class II · Z-0510-2019: Instructions for Use booklets were not included on the outer pouch
- Oct 17, 2018 · Class II · Z-0511-2019: Instructions for Use booklets were not included on the outer pouch

Source page: https://510kreport.com/device/K952984
Methodology: https://510kreport.com/methodology