# K962135: D.O.R.C. Microdiathermy System

- Pathway: 510(k) (Traditional)
- Applicant: Dutch Ophthalmic USA, Inc.
- Decided: Aug 29, 1996 after 87 days
- Product code: HQO (Unit, Cautery, Thermal, Ac-Powered)
- Device class: 2
- Regulation: 21 CFR 886.4115
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K990064: DI-Rhex Ophthalmic Diathermy System (1999), 0 descendants of its own

Source page: https://510kreport.com/device/K962135
Methodology: https://510kreport.com/methodology