# K010730: Modification to Flow 7000 Peripheral Vascular Coil

- Pathway: 510(k) (Traditional)
- Applicant: Usa Instruments, Inc.
- Decided: May 16, 2001 after 65 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.
4 later devices descend from it; 2 cite it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K023650: Insight Plus 9000 Phased Array Torso and Plevis Coil (2003), 2 descendants of its own
- K031172: Spirit Iii Totalsense Cardiac Coil (2003), 1 descendant of its own
- K042207: 11000 Rapture Phased Array Peripheral Vascular Coil (2004), 0 descendants of its own
- K033490: Spirit 5000 Cardiac Coil (2004), 0 descendants of its own

Source page: https://510kreport.com/device/K010730
Methodology: https://510kreport.com/methodology