# K002329: Pelvx Gellhorn Vaginal Pessary 603-608

- Pathway: 510(k) (Traditional)
- Applicant: Deschutes Medical Products, Inc.
- Decided: Sep 18, 2000 after 48 days
- Product code: HHW (Pessary, Vaginal)
- Device class: 2
- Regulation: 21 CFR 884.3575
- 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
- K012277: Portex Ring Pessary PVC-Non Sterile; Portex Ring Pessary Polythene- Non Sterile (2002), 0 descendants of its own

Source page: https://510kreport.com/device/K002329
Methodology: https://510kreport.com/methodology