# K964390: Chase Vessel Occluder

- Pathway: 510(k) (Traditional)
- Applicant: Chase Medical, Inc.
- Decided: Jan 31, 1997 after 88 days
- Product code: MJN (Catheter, Intravascular Occluding, Temporary)
- Device class: 2
- Regulation: 21 CFR 870.4450
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K883696 (1988). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K883696: Flo-Rester, Bio-Vascular, Inc. (1988) Summary page 1.

## Indications for use
The Vessel Occluder is intended to be used to internally occlude blood vessels during anastomosis.

Source page: https://510kreport.com/device/K964390
Methodology: https://510kreport.com/methodology