# K933008: Retractors and Scraper

- Pathway: 510(k) (Traditional)
- Applicant: Baxter Healthcare Corp
- Decided: Mar 11, 1994 after 263 days
- Product code: HET (Laparoscope, Gynecologic (And Accessories))
- Device class: 2
- Regulation: 21 CFR 884.1720
- 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.
1 of 4 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K092684: Laparoscopic Retractors (2010), 2 descendants of its own
- K112659: Surgical Retractors (2012), 0 descendants of its own
- K100442: Fastclamp Endoscopic Clamping System (2010), 0 descendants of its own

Source page: https://510kreport.com/device/K933008
Methodology: https://510kreport.com/methodology