# K891351: Newport Lateral Vaginal Retractor

- Pathway: 510(k) (Traditional)
- Applicant: Simpson/Basye, Inc.
- Decided: May 11, 1989 after 62 days
- Product code: KOH (Instrument, Manual, General Obstetric-Gynecologic)
- Device class: 1
- Regulation: 21 CFR 884.4520
- 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
- K991963: Patton Speculum (1999), 0 descendants of its own

Source page: https://510kreport.com/device/K891351
Methodology: https://510kreport.com/methodology