# K925079: Laparoscopic Inst. (Scissors,Forceps,Needleholder)

- Pathway: 510(k) (Traditional)
- Applicant: Endo Technic Corp.
- Decided: Aug 24, 1994 after 686 days
- Product code: HET (Laparoscope, Gynecologic (And Accessories))
- Device class: 2
- Regulation: 21 CFR 884.1720
- Recalls of this device: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device 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.

## Recalls of this device
- Jul 15, 2013 · Class II · Z-2264-2013: Multiple complaints reporting that the moveable jaw has broken during laparoscopic procedures.
- Jul 15, 2013 · Class II · Z-2265-2013: Multiple complaints reporting that the moveable jaw has broken during laparoscopic procedures.

Source page: https://510kreport.com/device/K925079
Methodology: https://510kreport.com/methodology