# K061950: HHF1 Echelon Multi-Purpose Coil

- Pathway: 510(k) (Abbreviated)
- Applicant: Hitachi Medical Systems America, Inc.
- Decided: Aug 18, 2006 after 39 days
- Product code: MOS (Coil, Magnetic Resonance, Specialty)
- 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: 6 generations back to K955249 (1995). 7 ancestors in all.
No later device cites it as a predicate yet.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K052172: HHF1 Magnetic Resonance Imaging System, Hitachi Medical Systems America, Inc. (2005) Summary page 4.

## Indications for use
Magnetic resonance imaging (MRI) and magnetic resonance angiography (MRA) of the musculoskeletal structures, soft tissue and vascular structures in various anatomic regions.

Source page: https://510kreport.com/device/K061950
Methodology: https://510kreport.com/methodology