# K973450: Sensor Pad

- Pathway: 510(k) (Traditional)
- Applicant: Inventive Products, Inc.
- Decided: Nov 14, 1997 after 64 days
- Product code: IYO (System, Imaging, Pulsed Echo, Ultrasonic)
- Device class: 2
- Regulation: 21 CFR 892.1560
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K955249 (1995). 1 ancestor in all.
23 later devices descend from it; 3 cite it directly.
0 of 25 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K955249: Sensor Pad, Inventive Products, Inc. (1995) Summary page 1.

## Most influential descendants
- K991469: Aware Pad (1999), 22 descendants of its own
- K023390: MY Breast Friend, Breast Self-Exam Pad (2002), 21 descendants of its own
- K050602: Altaire (2005), 17 descendants of its own
- K052172: HHF1 Magnetic Resonance Imaging System (2005), 16 descendants of its own
- K083533: Echelon C Mri System (2009), 11 descendants of its own

## Indications for use
The Sensor Pad is indicated as an aid for performing breast self-examination.

Source page: https://510kreport.com/device/K973450
Methodology: https://510kreport.com/methodology