# K840383: Menstrual Aspiration Kit

- Pathway: 510(k) (Traditional)
- Applicant: Intl. Medical Technologies, Inc.
- Decided: Apr 30, 1984 after 91 days
- Product code: HHI (System, Abortion, Vacuum)
- Device class: 2
- Regulation: 21 CFR 884.5070
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
20 later devices descend from it; 1 cites it directly.
0 of 21 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
- K132384: U-Scope 8000 System with HSC+Emb Cannula (2014), 19 descendants of its own
- K170660: Endosee Hysteroscope with Disposable Diagnostic (Dx) Cannula (2017), 5 descendants of its own
- K202445: Hystero-V Hysteroscope (2021), 4 descendants of its own
- K183020: Endosee System (2019), 4 descendants of its own
- K171113: LiNA OperaScope with HDMI cable and on-board LCD-single unit, LiNA OperaScope with HDMI cable and on-board LCD-6 units, LiNA OperaScope Recording Module (2018), 4 descendants of its own

Source page: https://510kreport.com/device/K840383
Methodology: https://510kreport.com/methodology