# K212864: dS TorsoCardiac 1.5T, dS MSK S 1.5T, dS MSK M 1.5T

- Pathway: 510(k) (Traditional)
- Applicant: Philips Healthcare (Suzhou) Co., Ltd.
- Decided: Dec 1, 2021 after 84 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: 4 generations back to K954190 (1995). 5 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K122897: Sense Head 16 Model 800647, Sense Spine 16 Model 800646; Sense Torso 16 Model 800645, Invivo Corporation (2012) Summary page 4.
- K120122: Sense MSK S 8CH 1.5T, Invivo Corporation (2012) Summary page 4.
- K111673: 1.5T and 3T 8-Channel Medium General Purpose Flex Coil, Invivo Corporation (2011) Summary page 4.

## Most influential descendants
- K232021: Smart Fit TorsoCardiac 1.5T and Smart Fit Shoulder 1.5T (2023), 1 descendant of its own
- K260519: Smart Fit TorsoCardiac 1.5T (2026), 0 descendants of its own

## Indications for use
The Magnetic Resonance (MR) coil is used with a Philips 1.5T MR scanner. A trained physician interprets the diagnostic images (of the anatomy of interest) produced.

Source page: https://510kreport.com/device/K212864
Methodology: https://510kreport.com/methodology