# K022304: Accumap Automatic Perimeter

- Pathway: 510(k) (Traditional)
- Applicant: Objectivision Pty, Ltd.
- Decided: Nov 14, 2003 after 486 days
- Product code: GWE (Stimulator, Photic, Evoked Response)
- Device class: 2
- Regulation: 21 CFR 882.1890
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K760199 (1976). 4 ancestors in all.
No later device cites it as a predicate yet.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K983983: Edi Veris System, Electro-Diagnostic Imaging, Inc. (1999) Summary page 1.

## Indications for use
The AccuMapB perimetry system uses multifocal recordings of visual evoked potentials as a diagnostic aid in the detection of glaucoma.

Source page: https://510kreport.com/device/K022304
Methodology: https://510kreport.com/methodology