# K040325: Panoret, Model PNM 60

- Pathway: 510(k) (Special)
- Applicant: Medibell Medical Vision Technologies, Ltd.
- Decided: Mar 8, 2004 after 27 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
Longest line of descent: 1 generation back to K001111 (2000). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K001111: Panoret, Model 1000A, Cmt Medical Technologies, Ltd. (2000)

## Indications for use
The PNM 60 is a diagnostic device indicated to provide digital photographs of the interior of the eye as well as the anterior segment and external part of the eye.

Source page: https://510kreport.com/device/K040325
Methodology: https://510kreport.com/methodology