# K082767: Kowa Nonmyd Alpha-Diii

- Pathway: 510(k) (Special)
- Applicant: Kowa Co., Ltd.
- Decided: Oct 21, 2008 after 29 days
- Product code: HKI (Camera, Ophthalmic, Ac-Powered)
- Device class: 2
- Regulation: 21 CFR 886.1120
- 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
- K083387: Modification to Kowa Nonmyd Alpha-Diii (2009), 1 descendant of its own
- K190056: KOWA VK-2s (2019), 0 descendants of its own

Source page: https://510kreport.com/device/K082767
Methodology: https://510kreport.com/methodology