# K020726: Dukal Disposable Vaginal Speculum, Small, Medium, and Large

- Pathway: 510(k) (Traditional)
- Applicant: Dukal Corp.
- Decided: May 15, 2002 after 70 days
- Product code: HIB (Speculum, Vaginal, Nonmetal)
- Device class: 2
- Regulation: 21 CFR 884.4530
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
3 later devices descend from it; 1 cites it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Medisul Disposable Vaginal Speculum: named in the summary without a submission number

## Most influential descendants
- K052314: Dynarex Vaginal Specula 4900, Models 4911-Small, 4912-Medium, 4913-Large (2005), 2 descendants of its own
- K072762: Depalt Vaginal Specuim and Depalt Lighting System (2008), 1 descendant of its own
- K133857: Brella-Spec (TM) Vaginal Speculum (2014), 0 descendants of its own

## Indications for use
The Dukal Disposable Vaginal Speculum is used to expose the interior of the vagina

Source page: https://510kreport.com/device/K020726
Methodology: https://510kreport.com/methodology