# K022157: RF Tent

- Pathway: 510(k) (Traditional)
- Applicant: Odin Medical Technologies, Ltd.
- Decided: Aug 28, 2002 after 57 days
- Product code: LNH (System, Nuclear Magnetic Resonance Imaging)
- Device class: 2
- Regulation: 21 CFR 892.1000
- 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 K002242 (2000). 1 ancestor in all.
1 later device descends from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K002242: Polestar N-10, Odin Technologies, Ltd. (2000) Summary page 1.
- (no number) installed copper sheeting: named in the summary without a submission number

## Most influential descendants
- K050237: Starshield V3 RF TRNT (2005), 0 descendants of its own

## Indications for use
The RF Tent is intended to create an area of substantially reduced Electromagnetic Interference (EMI) in the area enclosed by the RF Tent during image acquisition by the Polestar N-IO (K002242).

Source page: https://510kreport.com/device/K022157
Methodology: https://510kreport.com/methodology