# K911302: Models 5866-24M/5866-38M/5866-40M/6986M Adapt Kit

- Pathway: 510(k) (Traditional)
- Applicant: Medtronic Vascular
- Decided: Jul 30, 1991 after 127 days
- Product code: DTD (Pacemaker Lead Adaptor)
- Device class: 2
- Regulation: 21 CFR 870.3620
- Recalls of this device: none
- 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; 2 cite 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
- K132008: 6981M Lead Extender Kit, 6984M Lead Extender Kit, 6986M Lead Extender Kit, 5866-24M Lead Adaptor Kit, 5866-38M Lead Adap (2013), 0 descendants of its own
- K982220: Model 2872 Bipolar Lead Adaptor Kit (1998), 0 descendants of its own

Source page: https://510kreport.com/device/K911302
Methodology: https://510kreport.com/methodology