# K965185: Acrypak Folder

- Pathway: 510(k) (Traditional)
- Applicant: Alcon Laboratories
- Decided: Mar 31, 1997 after 97 days
- Product code: KYB (Lens, Guide, Intraocular)
- Device class: 1
- Regulation: 21 CFR 886.4300
- 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 K903574 (1990). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K913626: Softrans Injector, Staar Surgical Co. (1991) Summary page 2.
- K903574: Chiroflex Lens Microsert, Chiron Ophthalmics (1990) Summary page 2.

## Indications for use
The intended use of this device is to fold the Alcon ACRYSOF® intraocular lens prior to its insertion into the eye. The AcryPak® Folder is used as the folding forceps. A pair of implantation forceps is used to remove the folded lens from the AcryPak® Folder for lens implantation.

Source page: https://510kreport.com/device/K965185
Methodology: https://510kreport.com/methodology