# K894756: Denver Peritoneo-Venus Shunt

- Pathway: 510(k) (Traditional)
- Applicant: Codman & Shurtleff, Inc.
- Decided: Sep 29, 1989 after 64 days
- Product code: KPM (Shunt, Peritoneal)
- Device class: 2
- Regulation: 21 CFR 876.5955
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 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
- K973129: Denver Ascites Shunts, Denver Ascites Shunt Percutaneous Access Kits (1998), 0 descendants of its own

Source page: https://510kreport.com/device/K894756
Methodology: https://510kreport.com/methodology