# K813282: Synevac Vacuum Curettage Systems

- Pathway: 510(k) (Traditional)
- Applicant: Synemed, Inc.
- Decided: Dec 14, 1981 after 27 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.
6 later devices descend from it; 2 cite it directly.
0 of 7 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
- K030935: Berkeley V-10 Vacuum Curettage System (2003), 5 descendants of its own
- K093508: Rigid Cannulae Curved (RC6-RC12), Rigid Cannulae Straight (RS6-RS12) (2010), 2 descendants of its own
- K140213: Disposable Endoscopic Cannula (2015), 1 descendant of its own
- K251882: Uterine Aspiration Set (2025), 0 descendants of its own
- K172151: Hysteroscopy System (2018), 0 descendants of its own

Source page: https://510kreport.com/device/K813282
Methodology: https://510kreport.com/methodology