# K073352: Weberneedle Basic Laser

- Pathway: 510(k) (Traditional)
- Applicant: Weber Medical GmbH
- Decided: Aug 11, 2008 after 256 days
- Product code: ILY (Lamp, Infrared, Therapeutic Heating)
- Device class: 2
- Regulation: 21 CFR 890.5500
- 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 K033923 (2004). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K033923: TH0R Ddii IR Lamp System, Thor Intl. (2004) Summary page 1.
- K040662: Vectra Genisys (Module & Transportable) and Intelect XT (Module & Transportable) Laser Systems, Chattanooga Group (2004) Summary page 1.

## Indications for use
The weberneedledbasic laser is indicated to provide topical heating for the following: • temporary increase of local blood circulation. * temporary relief of minor muscle and joint aches, pains, and stiffness. * temporary relaxation of muscles. * temporary relief of muscle spasms. * temporary relief of minor pain and stiffness associated with arthritis.

Source page: https://510kreport.com/device/K073352
Methodology: https://510kreport.com/methodology