# K944129: Imagyn Laparoscopic Instruments

- Pathway: 510(k) (Traditional)
- Applicant: Imagyn Medical, Inc.
- Decided: Oct 20, 1994 after 57 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.
2 later devices descend from it; 1 cites it directly.
0 of 3 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
- K960748: Modified Hand Instrument Devices (1996), 1 descendant of its own
- K101101: Mini-Tong (2010), 0 descendants of its own

Source page: https://510kreport.com/device/K944129
Methodology: https://510kreport.com/methodology