# K112952: Ilwait Timer Oculopressor

- Pathway: 510(k) (Traditional)
- Applicant: Oryx Medical Pty, Ltd.
- Decided: May 10, 2012 after 218 days
- Product code: LCC (Applicator, Ocular Pressure)
- Device class: 2
- Regulation: 21 CFR 886.4610
- 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 K820526 (1982). 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)
- K820526: Relief Valve-Honan Intraoc. Pressure, The Lebanon Corp. (1982) Summary page 2.

## Indications for use
The ilwait timer oculopressor device is used to perform pre-operative ocular compression. The device is used in the clinical and pit-operative ward, when the patient is supine, sedated and accompanied by a medical staff member. The mass of the ilwait timer oculopressor provides even pressure across the eyelid to soften the eye. The timer function provides a reminder to monitor the compression duration

Source page: https://510kreport.com/device/K112952
Methodology: https://510kreport.com/methodology