# K231011: Merilas 532 shortpulse, Merilas 577 shortpulse, Merilas 810 shortpulse

- Pathway: 510(k) (Traditional)
- Applicant: Meridian AG
- Decided: Sep 12, 2023 after 155 days
- Product code: HQF (Laser, Ophthalmic)
- Device class: 2
- Regulation: 21 CFR 886.4390
- 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
The MERILAS 810 shortpulse laser is indicated for: - Photocoagulation - Iridotomy - Trabeculoplasty - Thermotherapy The MERILAS 532 shortpulse laser is indicated for: - Photocoagulation - Iridotomy - Trabeculoplasty The MERILAS 577 shortpulse laser is indicated for: - Photocoagulation - Iridotomy - Trabeculoplasty

Source page: https://510kreport.com/device/K231011
Methodology: https://510kreport.com/methodology