# K970882: Endolight End Irrigating Endo-Illuminator (20 GA. and 19 GA.)

- Pathway: 510(k) (Traditional)
- Applicant: American Medical Devices, Inc.
- Decided: Jun 24, 1997 after 106 days
- Product code: MPA (Endoilluminator)
- 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; 3 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. The FDA summary names no predicate by number.

## Most influential descendants
- K041108: Iscience Surgical Ophthalmic Microcannula (2004), 10 descendants of its own
- K080067: Iscience Interventional Ophthalmic Microcatheter (2008), 9 descendants of its own
- K173332: OMNI Surgical System (2017), 6 descendants of its own
- K202678: OMNI Surgical System (2021), 2 descendants of its own
- K991323: Smith & Nephew Subcutaneous Illuminator (1999), 2 descendants of its own

## Indications for use
For illumination and irrigation/aspiration during surgery.

Source page: https://510kreport.com/device/K970882
Methodology: https://510kreport.com/methodology