# K920662: Vascotwist 9/60

- Pathway: 510(k) (Traditional)
- Applicant: Vascor Medical Corp.
- Decided: Nov 24, 1993 after 649 days
- Product code: DTB (Permanent Pacemaker Electrode)
- Device class: 3
- Regulation: 21 CFR 870.3680
- 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; 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 lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K990483: Retrox RX 45-JBP 124774, 53-JBP 124775, 53-BP 124776, 60-124777 (1999), 1 descendant of its own
- K993139: YP 45/15-BP; YP 53/15-BP; YP 60/15-BP (1999), 0 descendants of its own

Source page: https://510kreport.com/device/K920662
Methodology: https://510kreport.com/methodology