# K073310: Oasis CTL Coil, OD Flexible Body Coil (L and XL), and Rapid Foot Coil

- Pathway: 510(k) (Abbreviated)
- Applicant: Hitachi Medical Corp.
- Decided: Jan 18, 2008 after 56 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
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) ECHELON Whole Spine (CTL) Coil: named in the summary without a submission number
- (no number) ALTAIRE Flex Body (Large) Coil: named in the summary without a submission number
- (no number) ALTAIRE Flex Body (Extra Large) Coil: named in the summary without a submission number
- (no number) OASIS RAPID Head Coil: named in the summary without a submission number

## Indications for use
The MR-CTL-1 20, OASIS CTL Coil is a recieve-only multiple array device used for MRI imaging of the human cervical spine, and thoracic spine. The MR-QFC-120, OASIS QOD Flexible Body Coil (L)is a recieve-only multiple array device used for MRI imaging of the abdomen. The MR-QFC-120, OASIS QD Flexible Body Coil (XL) is a recieve-only multiple array device used for MRI imaging of the abdomen. The MR-RFC-120, OASIS Rapid Foot Coil is a recieve-only multiple array device used for MRI imaging of the foot.

Source page: https://510kreport.com/device/K073310
Methodology: https://510kreport.com/methodology