# K070515: A-View Basic and Plus

- Pathway: 510(k) (Traditional)
- Applicant: Cordatec N.V.
- Decided: Jul 30, 2007 after 158 days
- Product code: ITX (Transducer, Ultrasonic, Diagnostic)
- Device class: 2
- Regulation: 21 CFR 892.1570
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 7 generations back to K935595 (1995). 47 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 49 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K052021: V5MS Transducer and MPT7-4 Multiplane Transesophageal Transducer, Siemens Medical Solutions USA, Inc. (2005) Summary page 1.
- K994373: Hdi 1500/SA 8800 Ultrasound System with Multiplane Transesophageal Ultrasound Transducer (MTP7-4), Atl Ultrasound, Inc. (2000) Summary page 1.
- K052517: Site-Rite 5 Ultrasound System, C.R. Bard, Inc. (2005) Summary page 1.
- (no number) Saline: named in the summary without a submission number

## Most influential descendants
- K170338: A-View (2017), 0 descendants of its own

## Indications for use
A-View Catheters are intended for use in conjunction with TEE investigation of the upper mediastinum in anaesthetised patients. They allow visibility of the distal ascending aorta by TEE and permit the condition of the ascending aorta to be evaluated before surgery. A-View Catheters are limited for use in adult patients.

Source page: https://510kreport.com/device/K070515
Methodology: https://510kreport.com/methodology