# K874706: Modified Simpson Peripheral Atherocath

- Pathway: 510(k) (Traditional)
- Applicant: Devices For Vascular Intervention, Inc.
- Decided: Jan 4, 1988 after 61 days
- Product code: LIT (Catheter, Angioplasty, Peripheral, Transluminal)
- Device class: 2
- Regulation: 21 CFR 870.1250
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
117 later devices descend from it; 1 cites it directly.
6 of 118 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
- K024243: Reform Peripheral Catheter System, Model 02200; Reform Peripheral Cathetercatheter, Model 02406 (2003), 116 descendants of its own
- K043553: Silverhawk Peripheral Plaque Excision System, Models 02550,04800, 05200, 02406, 04706, 04300 (2005), 79 descendants of its own
- K053460: Modification to Silverhawk Peripheral Plaque Excision System, Models 02550, 04800, 05200, 06002, 02406, 04706, 04300, (2006), 52 descendants of its own
- K061188: Silverhawk Peripheral Plaque Excision System (2006), 50 descendants of its own
- K061063: Modification to: Silverhawk Peripheral Plaque Excision System, Models P4028/FG08300 (2006), 37 descendants of its own

Source page: https://510kreport.com/device/K874706
Methodology: https://510kreport.com/methodology