# K011487: Correstore Patch, Models 1.5P2, 2P3, 3P4; Correstore Sizer, Model CRPS

- Pathway: 510(k) (Traditional)
- Applicant: Somanetics Corp.
- Decided: Nov 21, 2001 after 190 days
- Product code: DXZ (Patch, Pledget And Intracardiac, Petp, Ptfe, Polypropylene)
- Device class: 2
- Regulation: 21 CFR 870.3470
- 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
- K031586: Correstore Patch System (2003), 0 descendants of its own

Source page: https://510kreport.com/device/K011487
Methodology: https://510kreport.com/methodology