# K954943: Nevoscope

- Pathway: 510(k) (Traditional)
- Applicant: Nizar A. Mullani
- Decided: Mar 27, 1996 after 149 days
- Product code: KZF (Device, Medical Examination, Ac Powered)
- Device class: 1
- Regulation: 21 CFR 880.6320
- 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 K920103 (1992). 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)
- K920103: Episcope, Model 47300, Welch Allyn, Inc. (1992) Summary page 1.

## Indications for use
Nevoscope is a hand-held, skin examination microscope that is designed to view skin lesions by either surface illumination or transillumination.

Source page: https://510kreport.com/device/K954943
Methodology: https://510kreport.com/methodology