# K233742: CloudTMS Edge for OCD

- Pathway: 510(k) (Special)
- Applicant: Teleemg, LLC
- Decided: Dec 22, 2023 after 30 days
- Product code: QCI (Transcranial Magnetic Stimulation System For Obsessive-Compulsive Disorder)
- Device class: 2
- Regulation: 21 CFR 882.5802
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 10 generations back to DEN070003 (2008). 17 ancestors in all.
No later device cites it as a predicate yet.
0 of 18 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K221129: CloudTMS for OCD, Teleemg, LLC (2023) Summary page 5.

## Indications for use
The CloudTMS Edge for OCD is intended to be used as an adjunct for the treatment of adult patients suffering from Obsessive-Compulsive Disorder (OCD).

Source page: https://510kreport.com/device/K233742
Methodology: https://510kreport.com/methodology