# K000414: Medisul Disposable Vaginal Speculum

- Pathway: 510(k) (Abbreviated)
- Applicant: Marketing Perspectives
- Decided: Apr 4, 2000 after 56 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.
5 later devices descend from it; 3 cite it directly.
0 of 6 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
- K021017: Leespec Disposable Vaginal Speculum (2002), 1 descendant of its own
- K012535: DRG Disposable Vaginal Speculum (2002), 1 descendant of its own
- K052420: G-Spec Articulated Weighted Vaginal Speculum (2006), 0 descendants of its own
- K041757: Femspec Disposable Vaginal Speculum (2004), 0 descendants of its own
- K022948: Vaginal Speculum, Model 5555S, 5555M, or 5555L (2002), 0 descendants of its own

Source page: https://510kreport.com/device/K000414
Methodology: https://510kreport.com/methodology