# K103148: Aida Diagnostic Ultrasound System

- Pathway: 510(k) (Traditional)
- Applicant: Panasonic Healthcare Co., Ltd.
- Decided: Mar 11, 2011 after 137 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: 13 generations back to K894632 (1989). 91 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 94 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K093171: Viamo  Ssa-640A Version 1.2, Toshiba America Medical Systems, In.C (2009) Summary page 1.
- K081794: Model 7340 Ultrasound System, Esaote, S.p.A. (2008) Summary page 1.
- K022567: Sequoia Signature II Diagnostic Ultrasound System, Acuson Corp. (2002) Summary page 1.

## Most influential descendants
- K113612: Aida V1.5 Diagnostic Ultrasound System GM-72P00A (2012), 1 descendant of its own
- K122009: Aida VI.8 Diagnostic Ultrasound GM-72P00A, L13-5V1 Transducer (2012), 0 descendants of its own

## Indications for use
The AIDA diagnostic ultrasound system is intended for Peripheral Vessel applications. The system provides an automated intima-media thickness measurement of peripheral vessels such as the common carotid in the BIMT mode of operation for heart rate range of 20-150 beats per minute. The AIDA ultrasound system is contraindicated for fetal use.

Source page: https://510kreport.com/device/K103148
Methodology: https://510kreport.com/methodology