# K930933: Endopath Endoscopic Surgical Instruments

- Pathway: 510(k) (Traditional)
- Applicant: ETHICON, Inc.
- Decided: Jun 22, 1993 after 119 days
- Product code: GCJ (Laparoscope, General & Plastic Surgery)
- Device class: 2
- Regulation: 21 CFR 876.1500
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
14 later devices descend from it; 5 cite it directly.
0 of 15 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
- K061276: G-Prox Endoscopic Grasper (2006), 5 descendants of its own
- K061268: G-Lix Tissue Grasper (2006), 2 descendants of its own
- K012625: Reprocessed Unipolar Laparoscopic/Endoscopic Instruments (2001), 2 descendants of its own
- K100251: G-Cath Tissue Anchor Delivery Catheter, Models 205302, 205333 (2010), 1 descendant of its own
- K093018: G-Prox Endoscopic Grasper, Model 205333 (2009), 1 descendant of its own

Source page: https://510kreport.com/device/K930933
Methodology: https://510kreport.com/methodology