# K952232: Mrinnervu Disposable Endorectal Colon Coil, Catalong NO. PCC-15

- Pathway: 510(k) (Traditional)
- Applicant: Medrad, Inc.
- Decided: Jun 26, 1995 after 45 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
No predicates in its family tree.
4 later devices descend from it; 1 cites 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 lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K992193: Endo-Esophageal MR Coil (1999), 3 descendants of its own
- K994436: Surgi-Vision Esophageal Stylet Coil (2000), 2 descendants of its own
- K020790: Intercept Esophageal Internal MR Coil, Intercept Urethral Microcoil, and Intercept Vascular Internal MR Coil (2002), 0 descendants of its own
- K020495: Intercept Esophageal Internal MR Coil, Intercept Urethral Internal MR Coil, and Intercept Vascular Internal MR Coil (2002), 0 descendants of its own

Source page: https://510kreport.com/device/K952232
Methodology: https://510kreport.com/methodology