# K013820: Finn Chamber (R)

- Pathway: 510(k) (Traditional)
- Applicant: Epitest Ltd. OY
- Decided: Jan 30, 2002 after 75 days
- Product code: KXF (Applicator, Absorbent Tipped, Non-Sterile)
- Device class: 1
- Regulation: 21 CFR 880.6025
- 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 K811365 (1981). 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)
- K992553: IQ Chambers, Dormer Laboratories, Inc. (2000) Summary page 5.

## Indications for use
Finn Chamber® is an aluminum holding device to place allergens and allergen mixes in contact with the surface of skin during allergen patch testing. This product is intended for use by or under the supervision of a physician in the testing of individuals suspected of having allergies. It is not intended for over-the-counter use.

Source page: https://510kreport.com/device/K013820
Methodology: https://510kreport.com/methodology