# K033735: Vantage Pro Attenuation Correction Device

- Pathway: 510(k) (Traditional)
- Applicant: Adac Laboratories
- Decided: Dec 12, 2003 after 14 days
- Product code: KPS (System, Tomography, Computed, Emission)
- Device class: 2
- Regulation: 21 CFR 892.1200
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 3 generations back to K943596 (1995). 3 ancestors in all.
No later device cites it as a predicate yet.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K992078: Vantage Exspect II, Adac Laboratories (1999) Summary page 1.

## Indications for use
The Vantage Pro Attenuation Correction Device option to gamma camera systems marketed by ADAC, a Philips Medical Systems Company, produces images that depict the anatomical density of a patient. The system is intended to provide an enhancement to the emission images acquired using the gamma camera system by correcting for attenuation effects in the patient. Vantage Pro includes additional quality assurance tools to evaluate the resulting density image.

Source page: https://510kreport.com/device/K033735
Methodology: https://510kreport.com/methodology