# K013337: Prizm Keratome Blade (Nidek Model), Model MK8514NI

- Pathway: 510(k) (Traditional)
- Applicant: Surgin, Inc.
- Decided: Dec 13, 2001 after 65 days
- Product code: HNO (Keratome, Ac-Powered)
- Device class: 1
- Regulation: 21 CFR 886.4370
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
Prizm Blades are designed as replacement blades for Surgin's Nidek Model MK2000 keratome.

Source page: https://510kreport.com/device/K013337
Methodology: https://510kreport.com/methodology