# K023045: Microrupter V

- Pathway: 510(k) (Traditional)
- Applicant: Meridian AG
- Decided: Sep 26, 2002 after 14 days
- Product code: LXS (Laser, Neodymium:Yag, Ophthalmic For Posterior Capsulotomy And Cutting Pupilla)
- Device class: 2
- Regulation: 21 CFR 886.4392
- 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 K001511 (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)
- K001511: O-Las Ophthalmic Photodisruptor, A.R.C. Laser AG (2000) Summary page 1.

## Indications for use
This device will be used in ophthalmic applications, including: Posterior Capsulotomy Peripheral lridotomy Pupillary Membranectomy This device is intended for use by skilled Physicians and Healthcare Workers and may only be used under the supervision of a Physician. Federal law restricts this device to sale by or on the order of a licenced practioner

Source page: https://510kreport.com/device/K023045
Methodology: https://510kreport.com/methodology