# K121689: Vitascan LT Scanmaster

- Pathway: 510(k) (Traditional)
- Applicant: Vitacon Medical, Inc.
- Decided: Sep 19, 2012 after 104 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: 4 generations back to K915436 (1992). 7 ancestors in all.
No later device cites it as a predicate yet.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K093485: Vesiscan, Life-Tech, Inc. (2010) Summary page 1.
- K022153: Bladderscan Bvi 6100, Diagnostic Ultrasound Corp. (2002) Summary page 1.
- K071217: Bladderscan Bvi 9400 Ultrasound, Verathon Incorporated (2007) Summary page 7.

## Indications for use
The VitaScan LT (aka. Scanmaster) is a B-mode ultrasonic instrument which projects ultrasound energy through the lower abdomen of the non-pregnant patient to obtain an image of the bladder which is used to determine bladder volume non-invasively, on an intermittent basis.

Source page: https://510kreport.com/device/K121689
Methodology: https://510kreport.com/methodology