# K942002: Retractor

- Pathway: 510(k) (Traditional)
- Applicant: Automated Medical Products Corp.
- Decided: May 17, 1994 after 22 days
- Product code: GAD (Retractor)
- Device class: 1
- Regulation: 21 CFR 878.4800
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
4 later devices descend from it; 2 cite it directly.
0 of 5 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
- K133345: Reveel Endoscopic Retractor (2014), 2 descendants of its own
- K162445: LiVac Retractor System (2016), 1 descendant of its own
- K243399: Boehringer Laboratories Liver Retractor (2025), 0 descendants of its own
- K112659: Surgical Retractors (2012), 0 descendants of its own

Source page: https://510kreport.com/device/K942002
Methodology: https://510kreport.com/methodology